{"id":666,"date":"2019-09-26T12:34:32","date_gmt":"2019-09-26T09:34:32","guid":{"rendered":"https:\/\/sebhau.edu.ly\/colleges\/?p=666"},"modified":"2023-07-15T20:10:18","modified_gmt":"2023-07-15T17:10:18","slug":"description-courses-3","status":"publish","type":"post","link":"https:\/\/sebhau.edu.ly\/sc\/en\/description-courses-3\/","title":{"rendered":"\u0645\u062a\u0637\u0644\u0628\u0627\u062a \u0627\u0644\u062a\u062e\u0631\u062c"},"content":{"rendered":"

Course description, Department of Chemistry, College of Science, Sebha University<\/h2>\n

First: Undergraduate:<\/h3>\n\n\n\n\n\t\n\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t
The updated study plan of the Department of Chemistry for the spring of 2017<\/th><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n<\/thead>\n
<\/td><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n
\u0627\u0644\u0628\u0643\u0627\u0644\u0648\u0631\u064a\u0648\u0633 ( \u0627\u0644\u0625\u062c\u0627\u0632\u0629 \u0627\u0644\u062c\u0627\u0645\u0639\u064a\u0629 ) \u0641\u064a \u0639\u0644\u0648\u0645 \u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 (Chemistry \u00a0B.Sc. in)<\/td><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n
\u0645\u0643\u0648\u0646\u0627\u062a \u0627\u0644\u062e\u0637\u0629<\/td><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n
\u062a\u062a\u0643\u0648\u0646 \u0627\u0644\u062e\u0637\u0629 \u0627\u0644\u062f\u0631\u0627\u0633\u064a\u0629 \u0644\u062f\u0631\u062c\u0629 \u0627\u0644\u0628\u0643\u0627\u0644\u0648\u0631\u064a\u0648\u0633 ( \u0627\u0644\u0625\u062c\u0627\u0632\u0629 \u0627\u0644\u062c\u0627\u0645\u0639\u064a\u0629 ) \u0641\u064a \u0639\u0644\u0648\u0645 \u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0645\u0646 ( 147 ) \u0648\u062d\u062f\u0629 \u0645\u0639\u062a\u0645\u062f\u0629 \u0645\u0648\u0632\u0639\u0629 \u0639\u0644\u0649 \u0627\u0644\u0646\u062d\u0648 \u0627\u0644\u062a\u0627\u0644\u064a:<\/td><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n
\u0631.\u0645<\/td>The course<\/td><\/td><\/td><\/td><\/td><\/td>Credits<\/td>\n<\/tr>\n
1<\/td>Department requirements from the university (general requirements)<\/td><\/td><\/td><\/td><\/td><\/td>10<\/td>\n<\/tr>\n
2<\/td>Department Requirements from the College (Supporting Requirements)<\/td><\/td><\/td><\/td><\/td><\/td>29<\/td>\n<\/tr>\n
3<\/td>Department Specialized Requirements (Compulsory)<\/td><\/td><\/td><\/td><\/td><\/td>102<\/td>\n<\/tr>\n
4<\/td>\u0645\u062a\u0637\u0644\u0628\u0627\u062a \u0627\u0644\u0642\u0633\u0645 \u0627\u0644\u0627\u062e\u062a\u064a\u0627\u0631\u064a\u0629<\/td><\/td><\/td><\/td><\/td><\/td>6<\/td>\n<\/tr>\n
\u0627\u0644\u0645\u062c\u0645\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0648\u0639<\/td><\/td><\/td><\/td><\/td><\/td><\/td>147<\/td>\n<\/tr>\n
\u0623\u0648\u0644\u0627\u064b:-\u0627\u0644\u0645\u0642\u0631\u0631\u0627\u062a \u0627\u0644\u0639\u0627\u0645\u0629 (\u0627\u0644\u0645\u062a\u0637\u0644\u0628\u0627\u062a \u0627\u0644\u0639\u0627\u0645\u0629)<\/td><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n
\u0631.\u0645<\/td>Course Code<\/td>\u0627\u0633\u0645 \u0627\u0644\u0645\u0642\u0631\u0631 \u0628\u0627\u0644\u0639\u0631\u0628\u064a\u0629<\/td>\u0627\u0633\u0645 \u0627\u0644\u0645\u0642\u0631\u0631 \u0628\u0627\u0644\u0644\u063a\u0629 \u0627\u0644\u0627\u0646\u062c\u0644\u064a\u0632\u064a\u0629<\/td>Credits<\/td>\u0639\u062f\u062f \u0627\u0644\u0633\u0627\u0639\u0627\u062a<\/td><\/td>\u0627\u0644\u062a\u0631\u0627\u062a\u0628\u064a\u0629<\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td><\/td>theoretical<\/td>Practice<\/td><\/td>\n<\/tr>\n
1<\/td>Arb101<\/td>\u0627\u0644\u0644\u063a\u0629 \u0627\u0644\u0639\u0631\u0628\u064a\u0629 \u0623<\/td>Arabic language A<\/td>2<\/td>2<\/td>\\<\/td>\/<\/td>\n<\/tr>\n
2<\/td>Arb201<\/td>\u0627\u0644\u0644\u063a\u0629 \u0627\u0644\u0639\u0631\u0628\u064a\u0629 \u0628<\/td>Arabic language B<\/td>2<\/td>2<\/td>\\<\/td>Arb101<\/td>\n<\/tr>\n
3<\/td>HLY401<\/td>\u062a\u0627\u0631\u064a\u062e \u0644\u064a\u0628\u064a\u0627<\/td>History of Libya<\/td>2<\/td>2<\/td>\\<\/td>HSCI301<\/td>\n<\/tr>\n
4<\/td>En 101<\/td>\u0627\u0644\u0644\u063a\u0629 \u0627\u0644\u0625\u0646\u062c\u0644\u064a\u0632\u064a\u0629 \u0623<\/td>English language A<\/td>2<\/td>2<\/td>\\<\/td>\/<\/td>\n<\/tr>\n
5<\/td>En 201<\/td>\u0627\u0644\u0644\u063a\u0629 \u0627\u0644\u0625\u0646\u062c\u0644\u064a\u0632\u064a\u0629 \u0628<\/td>English language B<\/td>2<\/td>2<\/td>\\<\/td>En 101<\/td>\n<\/tr>\n
\u0627\u0644\u0645\u062c\u0645\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0648\u0639<\/td><\/td><\/td><\/td>10<\/td>10\u00a0<\/td>\u00a0\\<\/td><\/td>\n<\/tr>\n
\u0623\u0648\u0644\u0627\u064b:-\u0627\u0644\u0645\u0642\u0631\u0631\u0627\u062a \u0627\u0644\u062f\u0627\u0639\u0645\u0629 \u0648\u0627\u0644\u0645\u0633\u0627\u0646\u062f\u0629<\/td><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n
\u0631.\u0645<\/td>Course Code<\/td>\u0627\u0633\u0645 \u0627\u0644\u0645\u0642\u0631\u0631 \u0628\u0627\u0644\u0639\u0631\u0628\u064a\u0629<\/td>\u0627\u0633\u0645 \u0627\u0644\u0645\u0642\u0631\u0631 \u0628\u0627\u0644\u0644\u063a\u0629 \u0627\u0644\u0627\u0646\u062c\u0644\u064a\u0632\u064a\u0629<\/td>Credits<\/td>\u0639\u062f\u062f \u0627\u0644\u0633\u0627\u0639\u0627\u062a<\/td><\/td>\u0627\u0644\u062a\u0631\u0627\u062a\u0628\u064a\u0629<\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td><\/td>theoretical<\/td>Practice<\/td><\/td>\n<\/tr>\n
1<\/td>MA \u2013 100<\/td>\u0631\u064a\u0627\u0636\u0629 \u0639\u0627\u0645\u0629<\/td>General Mathematics<\/td>4<\/td>4<\/td>\u2013<\/td>\u2013<\/td>\n<\/tr>\n
2<\/td>MA \u2013 200<\/td>\u0647\u0646\u062f\u0633\u0629 \u062a\u062d\u0644\u064a\u0644\u064a\u0629<\/td>Geometry & velocity<\/td>3<\/td>3<\/td>\u2013<\/td>MA - 100<\/td>\n<\/tr>\n
3<\/td>MA \u2013 300<\/td>\u062a\u0641\u0627\u0636\u0644, \u062a\u0643\u0627\u0645\u0644 \u0648 \u0645\u062d\u062f\u062f\u0627\u062a<\/td>Calculus, Integration & Limits<\/td>3<\/td>3<\/td>\u2013<\/td>MA - 200<\/td>\n<\/tr>\n
4<\/td>PH- 101<\/td>\u0645\u0642\u062f\u0645\u0629 \u0641\u064a \u0627\u0644\u0641\u064a\u0632\u064a\u0627\u0621<\/td>Introductory Physics<\/td>3<\/td>3<\/td>\u2013<\/td>\u2013<\/td>\n<\/tr>\n
5<\/td>CS \u2013 101<\/td>\u0645\u0642\u062f\u0645\u0629 \u0641\u064a \u0627\u0644\u062d\u0627\u0633\u0648\u0628<\/td>Introd. to Computer Science<\/td>3<\/td>3<\/td>\u2013<\/td>\u2013<\/td>\n<\/tr>\n
6<\/td>ZY \u2013 101<\/td>\u0639\u0644\u0645 \u062d\u064a\u0648\u0627\u0646 \u0639\u0627\u0645<\/td>General Zoology<\/td>2<\/td>2<\/td>\u2013<\/td>\u2013<\/td>\n<\/tr>\n
7<\/td>ZY \u2013 111<\/td>\u0639\u0644\u0645 \u062d\u064a\u0648\u0627\u0646 \u0639\u0627\u0645 \u0627\u0644\u0645\u0639\u0645\u0644\u064a<\/td>Practical Zoology<\/td>1<\/td>\u2013<\/td>4<\/td>\u2013<\/td>\n<\/tr>\n
8<\/td>BT \u2013 101<\/td>\u0639\u0644\u0645 \u0646\u0628\u0627\u062a \u0639\u0627\u0645<\/td>General Botany<\/td>2<\/td>2<\/td>\u2013<\/td>\u2013<\/td>\n<\/tr>\n
9<\/td>BT \u2013 111<\/td>\u0639\u0644\u0645 \u0646\u0628\u0627\u062a \u0639\u0627\u0645 \u0627\u0644\u0645\u0639\u0645\u0644\u064a<\/td>Practical Botany<\/td>1<\/td>\u2013<\/td>4<\/td>\u2013<\/td>\n<\/tr>\n
10<\/td>ES \u2013 101<\/td>\u0639\u0644\u0645 \u0627\u0644\u0623\u0631\u0636 \u0627\u0644\u0639\u0627\u0645<\/td>General Geology<\/td>2<\/td>2<\/td>\u2013<\/td>\u2013<\/td>\n<\/tr>\n
11<\/td>ES \u2013 111<\/td>\u0639\u0644\u0645 \u0627\u0644\u0623\u0631\u0636 \u0639\u0627\u0645 \u0627\u0644\u0639\u0645\u0644\u064a<\/td>Practical Geology<\/td>1<\/td>\u2013<\/td>4<\/td>\u2013<\/td>\n<\/tr>\n
12<\/td>HSCI- 301<\/td>\u062a\u0627\u0631\u064a\u062e \u0627\u0644\u0639\u0644\u0648\u0645<\/td>History of science<\/td>2<\/td>2<\/td>\u2013<\/td>Arb201<\/td>\n<\/tr>\n
13<\/td>En -301<\/td>\u0627\u0644\u0644\u063a\u0629 \u0627\u0644\u0625\u0646\u062c\u0644\u064a\u0632\u064a\u0629 \u062c<\/td>English language C<\/td>2<\/td>2<\/td>\u2013<\/td>En 201<\/td>\n<\/tr>\n
\u0627\u0644\u0645\u062c\u0645\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0648\u0639<\/td><\/td><\/td><\/td>29<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n
\u00a0\u062b\u0627\u0646\u064a\u0627 :- \u0645\u062a\u0637\u0644\u0628\u0627\u062a \u0627\u0644\u0642\u0633\u0645 \u0627\u0644\u062a\u062e\u0635\u0635\u064a\u0629 (\u0627\u0644\u0625\u062c\u0628\u0627\u0631\u064a\u0629)<\/td><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n
\u0631.\u0645<\/td>Course Code<\/td>\u0627\u0633\u0645 \u0627\u0644\u0645\u0642\u0631\u0631 \u0628\u0627\u0644\u0639\u0631\u0628\u064a\u0629<\/td>\u0627\u0633\u0645 \u0627\u0644\u0645\u0642\u0631\u0631 \u0628\u0627\u0644\u0644\u063a\u0629 \u0627\u0644\u0627\u0646\u062c\u0644\u064a\u0632\u064a\u0629<\/td>Credits<\/td>\u0639\u062f\u062f \u0627\u0644\u0633\u0627\u0639\u0627\u062a<\/td><\/td>\u0627\u0644\u062a\u0631\u0627\u062a\u0628\u064a\u0629<\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td><\/td>theoretical<\/td>Practice<\/td><\/td>\n<\/tr>\n
1<\/td>CH- 100<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0639\u0627\u0645\u0629<\/td>General Chemistry<\/td>2<\/td>2<\/td><\/td>\u2013<\/td>\n<\/tr>\n
2<\/td>CH \u2013 111<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0639\u0627\u0645\u0629 \u0639\u0645\u0644\u064a<\/td>Practical General Chemistry<\/td>1<\/td>\u2013<\/td>4<\/td>\u2013<\/td>\n<\/tr>\n
3<\/td>CH \u2013 201<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u062a\u062d\u0644\u064a\u0644\u064a\u0629 \u0639\u0627\u0645\u0629<\/td>General Analytical chemistry<\/td>2<\/td>2<\/td>\u2013<\/td>CH- 100<\/td>\n<\/tr>\n
4<\/td>CH \u2013202<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u063a\u064a\u0631 \u0639\u0636\u0648\u064a\u0629 \u0639\u0627\u0645\u0629<\/td>General inorganic chemistry<\/td>2<\/td>2<\/td>\u2013<\/td>CH- 100<\/td>\n<\/tr>\n
5<\/td>CH \u2013 203<\/td>\u0645\u0628\u0627\u062f\u0626 \u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0639\u0636\u0648\u064a\u0629<\/td>Fund. of organic Chemistry<\/td>3<\/td>3<\/td>\u2013<\/td>CH- 100<\/td>\n<\/tr>\n
6<\/td>CH \u2013 204<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0641\u064a\u0632\u064a\u0627\u0626\u064a\u0629 \u0639\u0627\u0645\u0629<\/td>General Physical Chemistry<\/td>3<\/td>3<\/td>4<\/td>CH- 100<\/td>\n<\/tr>\n
7<\/td>CH \u2013 211<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u062a\u062d\u0644\u064a\u0644\u064a\u0629 \u0639\u0627\u0645\u0629 \u0639\u0645\u0644\u064a<\/td>Practical Analytical chemistry<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013111<\/td>\n<\/tr>\n
8<\/td>CH \u2013212<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u063a\u064a\u0631 \u0639\u0636\u0648\u064a\u0629 \u0639\u0645\u0644\u064a<\/td>Practical inorganic chemistry<\/td>1<\/td>\u00ad\u2013<\/td>4<\/td>CH \u2013 111<\/td>\n<\/tr>\n
9<\/td>CH \u2013214<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0641\u064a\u0632\u064a\u0627\u0626\u064a\u0629 \u0639\u0627\u0645\u0629 \u0639\u0645\u0644\u064a<\/td>Practical Physical chemistry I<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 111<\/td>\n<\/tr>\n
10<\/td>CH \u2013 301<\/td>\u0627\u0644\u0645\u0639\u0627\u064a\u0631\u0627\u062a \u0648\u0627\u0644\u0637\u0631\u0642 \u0627\u0644\u0648\u0632\u0646\u064a\u0629 \u0627\u0644\u0639\u0645\u0644\u064a<\/td>Titrimetric & Gravimetric methods<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 201, CH \u2013 211<\/td>\n<\/tr>\n
11<\/td>CH \u2013 302<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0639\u0646\u0627\u0635\u0631 \u0627\u0644\u0645\u0645\u062b\u0644\u0629<\/td>Chemistry of Representative<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 202, CH \u2013 212<\/td>\n<\/tr>\n
12<\/td>CH \u2013 303<\/td>\u0627\u0644\u0645\u062c\u0645\u0648\u0639\u0627\u062a \u0627\u0644\u0648\u0638\u064a\u0641\u0629 \u0627\u0644\u0639\u0636\u0648\u064a\u0629<\/td>Organic Functional Groups<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 203<\/td>\n<\/tr>\n
13<\/td>CH \u2013 304<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0641\u064a\u0632\u064a\u0627\u0626\u064a\u0629 \u0639\u0627\u0645\u0629 II<\/td>General Physical Chemistry - II<\/td>3<\/td>3<\/td>\u2013<\/td>CH \u2013 204, CH \u2013 214<\/td>\n<\/tr>\n
14<\/td>CH \u2013 311<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u062a\u062d\u0644\u064a\u0644\u064a\u0629 \u0639\u0645\u0644\u064a II<\/td>Practical analytical chemistry II<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 201, CH \u2013 211<\/td>\n<\/tr>\n
15<\/td>CH \u2013 312<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u063a\u064a\u0631 \u0639\u0636\u0648\u064a\u0629 \u0639\u0645\u0644\u064a II<\/td>Practical inorganic chemistry II<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 202, CH \u2013 212<\/td>\n<\/tr>\n
16<\/td>CH \u2013 313<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u063a\u064a\u0631 \u0639\u0636\u0648\u064a\u0629 \u0639\u0645\u0644\u064a II<\/td>Practical organic chemistry II<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 203<\/td>\n<\/tr>\n
17<\/td>CH \u2013 314<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0641\u064a\u0632\u064a\u0627\u0626\u064a\u0629 \u0639\u0627\u0645\u0629 \u0639\u0645\u0644\u064a II<\/td>Practical Physical chemistry II<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 204, CH \u2013 214<\/td>\n<\/tr>\n
18<\/td>CH \u2013 400<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0631\u064a\u0627\u0636\u064a\u0629<\/td>Mathematics for chemistry<\/td>2<\/td>2<\/td>\u2013<\/td>MA200<\/td>\n<\/tr>\n
19<\/td>CH \u2013 401<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0637\u0631\u0627\u0626\u0642 \u0627\u0644\u0641\u0635\u0644<\/td>Separation techniques<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 301, CH \u2013 311<\/td>\n<\/tr>\n
20<\/td>CH \u2013 402<\/td>\u0627\u0644\u062a\u0631\u0627\u0628\u0637 \u0648\u0627\u0644\u062a\u0631\u0643\u064a\u0628 \u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0626\u064a<\/td>Bonding and Chemical Structure<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 302, CH \u2013 312<\/td>\n<\/tr>\n
21<\/td>CH \u2013 403<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0645\u0631\u0643\u0628\u0627\u062a \u0627\u0644\u0639\u0637\u0631\u064a\u0629<\/td>Chemistry of Aromatic Compounds<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 303<\/td>\n<\/tr>\n
22<\/td>CH \u2013 404<\/td>\u0627\u0644\u062f\u064a\u0646\u0627\u0645\u064a\u0643\u0627 \u0627\u0644\u062d\u0631\u0627\u0631\u064a\u0629 \u0648\u0627\u0644\u0627\u062a\u0632\u0627\u0646<\/td>Thermodynamics and equilibrium<\/td>3<\/td>3<\/td>\u2013<\/td>CH \u2013 304, CH \u2013 314<\/td>\n<\/tr>\n
23<\/td>CH \u2013 411<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0637\u0631\u0627\u0626\u0642 \u0627\u0644\u0641\u0635\u0644 \u0627\u0644\u0639\u0645\u0644\u064a<\/td>Practical Separation techniques<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 301, CH \u2013 311<\/td>\n<\/tr>\n
24<\/td>CH \u2013 412<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u063a\u064a\u0631 \u0639\u0636\u0648\u064a\u0629 \u0639\u0645\u0644\u064a III<\/td>Practical inorganic chemistry III<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 302, CH \u2013 312<\/td>\n<\/tr>\n
25<\/td>CH \u2013 413<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0645\u0631\u0643\u0628\u0627\u062a \u0627\u0644\u0639\u0637\u0631\u064a\u0629 \u0627\u0644\u0639\u0645\u0644\u064a<\/td>Practical Aromatic Chemistry<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 303<\/td>\n<\/tr>\n
26<\/td>CH \u2013 414<\/td>\u0627\u0644\u062f\u064a\u0646\u0627\u0645\u064a\u0643\u0627 \u0627\u0644\u062d\u0631\u0627\u0631\u064a\u0629 \u0627\u0644\u0639\u0645\u0644\u064a<\/td>Practical Thermodynamics chemistry<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 304, CH \u2013 314<\/td>\n<\/tr>\n
27<\/td>CH \u2013 500<\/td>\u0627\u0644\u0641\u064a\u0632\u064a\u0627\u0621 \u0627\u0644\u062d\u0631\u0627\u0631\u064a\u0629<\/td>Thermo-physics<\/td>3<\/td>3<\/td>\u2013<\/td>PH-101<\/td>\n<\/tr>\n
28<\/td>CH \u2013 501<\/td>\u0637\u0631\u0627\u0626\u0642 \u0627\u0644\u062a\u062d\u0644\u064a\u0644 \u0627\u0644\u0643\u0647\u0631\u0628\u064a\u0629<\/td>Electro analytical techniques<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 401, CH \u2013 411<\/td>\n<\/tr>\n
29<\/td>CH \u2013 502<\/td>\u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u062a\u0646\u0627\u0633\u0642\u064a\u0629<\/td>Coordination Chemistry<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 402, CH \u2013 412<\/td>\n<\/tr>\n
30<\/td>CH \u2013 503<\/td>\u0645\u064a\u0643\u0627\u0646\u064a\u0643\u0627 \u0627\u0644\u062a\u0641\u0627\u0639\u0644\u0627\u062a \u0627\u0644\u0639\u0636\u0648\u064a\u0629<\/td>Reaction Mechanism<\/td>3<\/td>3<\/td>\u2013<\/td>CH \u2013 403, CH \u2013 413<\/td>\n<\/tr>\n
31<\/td>CH \u2013 504<\/td>\u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0636\u0648\u0626\u064a\u0629 , \u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u062d\u0631\u0643\u064a\u0629 \u0648 \u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0643\u0647\u0631\u0628\u064a\u0629<\/td>Chemical kinetics, Photochemistry and Electrochemistry<\/td>3<\/td>3<\/td>\u2013<\/td>CH \u2013 404, CH \u2013 414<\/td>\n<\/tr>\n
32<\/td>CH \u2013 505<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0635\u0646\u0627\u0639\u064a\u0629 \u0644\u0644\u0628\u0648\u0644\u064a\u0645\u0631\u0627\u062a<\/td>Polymer Technology<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 403, CH \u2013 413<\/td>\n<\/tr>\n
33<\/td>CH \u2013 511<\/td>\u0637\u0631\u0627\u0626\u0642 \u0627\u0644\u0639\u0645\u0644\u064a\u0629 \u0644\u0644\u062a\u062d\u0644\u064a\u0644 \u0627\u0644\u0643\u0647\u0631\u0628\u064a<\/td>Practical Electrochemistry<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 401, CH \u2013 411<\/td>\n<\/tr>\n
34<\/td>CH \u2013 512<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u063a\u064a\u0631 \u0639\u0636\u0648\u064a\u0629 \u0639\u0645\u0644\u064a IV<\/td>Practical inorganic chemistry IV<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 402, CH \u2013 412<\/td>\n<\/tr>\n
35<\/td>CH - 513<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0639\u0636\u0648\u064a\u0629 \u0639\u0645\u0644\u064a III<\/td>Practical organic chemistry III<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 403, CH \u2013 413<\/td>\n<\/tr>\n
36<\/td>CH \u2013 514<\/td>\u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0636\u0648\u0626\u064a\u0629 , \u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u062d\u0631\u0643\u064a\u0629 \u0648 \u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0643\u0647\u0631\u0628\u064a\u0629<\/td>Practical Electrochemistry<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 404, CH \u2013 414<\/td>\n<\/tr>\n
37<\/td>CH \u2013 515<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0639\u0645\u0644\u064a\u0629 \u0644\u0644\u0628\u0648\u0644\u064a\u0645\u0631\u0627\u062a<\/td>Practical Polymer chemistry<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 403, CH \u2013 413<\/td>\n<\/tr>\n
38<\/td>CH - 508<\/td>\u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u062d\u064a\u0648\u064a\u0629<\/td>Biochemistry<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 403, CH \u2013 413<\/td>\n<\/tr>\n
39<\/td>CH \u2013 601<\/td>\u0637\u0631\u0642 \u0627\u0644\u062a\u062d\u0644\u064a\u0644 \u0627\u0644\u0637\u064a\u0641\u064a<\/td>Spectroscopic Methods\u00a0of analysis<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 501, CH \u2013 511<\/td>\n<\/tr>\n
40<\/td>CH \u2013 602<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0639\u0646\u0627\u0635\u0631 \u0627\u0644\u0627\u0646\u062a\u0642\u0627\u0644\u064a\u0629<\/td>Chemistry of Non-Metals<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 502, CH \u2013 512<\/td>\n<\/tr>\n
41<\/td>CH \u2013 603<\/td>\u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0641\u0631\u0627\u063a\u064a\u0629 \u0648\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0645\u0646\u062a\u062c\u0627\u062a \u0627\u0644\u0637\u0628\u064a\u0639\u064a\u0629<\/td>Stereochemistry and Natural products<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 503, CH \u2013 513<\/td>\n<\/tr>\n
42<\/td>CH \u2013 604<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0643\u0645 \u0648\u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0646\u0648\u0648\u064a\u0629<\/td>Quantum & Nuclear Chemistry<\/td>3<\/td>3<\/td>\u2013<\/td>CH \u2013 504, CH \u2013 514<\/td>\n<\/tr>\n
43<\/td>CH \u2013 605<\/td>\u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0635\u0646\u0627\u0639\u064a\u0629 \u0627\u0644\u0646\u0641\u0637\u064a\u0629<\/td>petrochemical industry<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 505, CH \u2013 515<\/td>\n<\/tr>\n
44<\/td>CH \u2013 611<\/td>\u0637\u0631\u0642 \u0627\u0644\u0639\u0645\u0644\u064a\u0629 \u0641\u064a \u0627\u0644\u062a\u062d\u0644\u064a\u0644 \u0627\u0644\u0637\u064a\u0641\u064a I<\/td>Practical Spectroscopic analysis I<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 501, CH \u2013 511<\/td>\n<\/tr>\n
45<\/td>CH \u2013 612<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u063a\u064a\u0631 \u0639\u0636\u0648\u064a\u0629 \u0639\u0645\u0644\u064a V<\/td>Practical inorganic chemistry V<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 502, CH \u2013 512<\/td>\n<\/tr>\n
46<\/td>CH \u2013 613<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0639\u0636\u0648\u064a\u0629 \u0639\u0645\u0644\u064a IV<\/td>Practical organic chemistry IV<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 503, CH \u2013 513<\/td>\n<\/tr>\n
47<\/td>CH \u2013 614<\/td>\u0627\u0644\u062d\u0648\u0633\u0628\u0629 \u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0626\u064a\u0629<\/td>Practical theoretical Chemistry<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 504, CH \u2013 514<\/td>\n<\/tr>\n
48<\/td>CH \u2013 615<\/td>\u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0646\u0641\u0637\u064a\u0629 \u0627\u0644\u0645\u0639\u0645\u0644\u064a\u0629<\/td>Practical Petroleum Chemistry<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 505, CH \u2013 515<\/td>\n<\/tr>\n
49<\/td>CH \u2013 701<\/td>\u0637\u0631\u0642 \u0627\u0644\u062a\u062d\u0644\u064a\u0644 \u0627\u0644\u0622\u0644\u064a<\/td>instrumental method of analysis<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 601, CH \u2013 611<\/td>\n<\/tr>\n
50<\/td>CH \u2013 702<\/td>\u0645\u064a\u0643\u0627\u0646\u064a\u0643\u0627 \u0627\u0644\u062a\u0641\u0627\u0639\u0644\u0627\u062a \u0627\u0644\u063a\u064a\u0631 \u0639\u0636\u0648\u064a\u0629<\/td>Inorganic Reaction Mechanism<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 602, CH \u2013 612<\/td>\n<\/tr>\n
51<\/td>CH \u2013 703<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0645\u0631\u0643\u0628\u0627\u062a \u0627\u0644\u062d\u0644\u0642\u064a\u0629 \u0648\u0627\u0644\u0623\u0637\u064a\u0627\u0641<\/td>Heterocyclic Compounds & Spectroscopy<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 603, CH \u2013 613<\/td>\n<\/tr>\n
52<\/td>CH \u2013 704<\/td>\u0627\u0644\u0623\u0637\u064a\u0627\u0641 \u0627\u0644\u062c\u0632\u0626\u064a\u0629 \u0648\u0627\u0644\u062f\u064a\u0646\u0627\u0645\u064a\u0643 \u0627\u0644\u0625\u062d\u0635\u0627\u0626\u064a \u0648\u0627\u0644\u062d\u0627\u0644\u0629 \u0627\u0644\u0635\u0644\u0628\u0629<\/td>Molecular Spectra, Statically Thermodynamics and Solid State<\/td>3<\/td>3<\/td>\u2013<\/td>CH \u2013 604, CH \u2013 614<\/td>\n<\/tr>\n
53<\/td>CH \u2013 705<\/td>\u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0635\u0646\u0627\u0639\u064a\u0629 \u0627\u0644\u062a\u0637\u0628\u064a\u0642\u064a\u0629<\/td>Applied Chemistry<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 605, CH \u2013 615<\/td>\n<\/tr>\n
54<\/td>CH \u2013 707<\/td>\u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0635\u0646\u0627\u0639\u064a\u0629 \u0627\u0644\u063a\u064a\u0631 \u0639\u0636\u0648\u064a\u0629<\/td>Industrial Inorganic Chemistry<\/td>2<\/td>2<\/td>\u2013<\/td>CH \u2013 502, CH \u2013 502<\/td>\n<\/tr>\n
55<\/td>CH \u2013 711<\/td>\u0637\u0631\u0642 \u0627\u0644\u0639\u0645\u0644\u064a\u0629 \u0644\u0644\u062a\u062d\u0644\u064a\u0644 \u0627\u0644\u0637\u064a\u0641\u064a II<\/td>Practical Spectroscopic analysis II<\/td>1<\/td>-<\/td>4<\/td>CH \u2013 601, CH \u2013 611<\/td>\n<\/tr>\n
56<\/td>CH \u2013 712<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u063a\u064a\u0631 \u0639\u0636\u0648\u064a\u0629 \u0639\u0645\u0644\u064a IV<\/td>Practical inorganic chemistry IV<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 602, CH \u2013 612<\/td>\n<\/tr>\n
57<\/td>CH \u2013 713<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0639\u0636\u0648\u064a\u0629 \u0639\u0645\u0644\u064aIV<\/td>Practical organic chemistry V<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 603, CH \u2013 613<\/td>\n<\/tr>\n
58<\/td>CH \u2013 715<\/td>\u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0635\u0646\u0627\u0639\u064a\u0629 \u0627\u0644\u0645\u0639\u0645\u0644\u064a\u0629<\/td>Practical Industrial Chemistry<\/td>1<\/td>\u2013<\/td>4<\/td>CH \u2013 605, CH \u2013 615<\/td>\n<\/tr>\n
59<\/td>CH \u2013 700<\/td>\u0637\u0631\u0642 \u0628\u062d\u062b<\/td>Research methodology<\/td>1<\/td>2<\/td>-<\/td><\/td>\n<\/tr>\n
60<\/td>CH \u2013 800<\/td>\u0645\u0634\u0631\u0648\u0639 \u0628\u062d\u062b<\/td>Project<\/td>3<\/td>3<\/td>\u2013<\/td><\/td>\n<\/tr>\n
\u0627\u0644\u0645\u062c\u0645\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0648\u0639<\/td><\/td><\/td><\/td>103<\/td><\/td><\/td><\/td>\n<\/tr>\n
\u00a0\u00a0 \u062b\u0627\u0644\u062b\u0627:-\u0645\u062a\u0637\u0644\u0628\u0627\u062a \u0627\u0644\u0642\u0633\u0645 \u0627\u0644\u0627\u062e\u062a\u064a\u0627\u0631\u064a\u0629<\/td><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n
\u064a\u0643\u0648\u0646 \u0627\u0644\u0637\u0627\u0644\u0628 \u0645\u0644\u0632\u0645 \u0628\u0627\u062e\u062a\u064a\u0627\u0631 8 ( \u0648\u062d\u062f\u0627\u062a \u062f\u0631\u0627\u0633\u064a\u0629 ) \u062e\u0644\u0627\u0644 \u0641\u062a\u0631\u0629 \u062f\u0631\u0627\u0633\u062a\u0647 \u0645\u0646 \u0627\u0644\u0645\u0642\u0631\u0631\u0627\u062a \u0627\u0644\u0627\u062a\u064a\u0629<\/td><\/td><\/td><\/td><\/td><\/td><\/td><\/td>\n<\/tr>\n
\u0631.\u0645<\/td>Course Code<\/td>\u0627\u0633\u0645 \u0627\u0644\u0645\u0642\u0631\u0631 \u0628\u0627\u0644\u0639\u0631\u0628\u064a\u0629<\/td>\u0627\u0633\u0645 \u0627\u0644\u0645\u0642\u0631\u0631 \u0628\u0627\u0644\u0644\u063a\u0629 \u0627\u0644\u0627\u0646\u062c\u0644\u064a\u0632\u064a\u0629<\/td>Credits<\/td>\u0639\u062f\u062f \u0627\u0644\u0633\u0627\u0639\u0627\u062a<\/td>\u0627\u0644\u062a\u0631\u0627\u062a\u0628\u064a\u0629<\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td><\/td>theoretical<\/td><\/td><\/td>\n<\/tr>\n
1<\/td>CH \u2013 801<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0628\u064a\u0626\u0629<\/td>Environmental\u00a0chemistry<\/td>2<\/td>2<\/td>CH-701<\/td><\/td>\n<\/tr>\n
2<\/td>CH \u2013 821<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0645\u0627\u0621 \u0648\u0627\u0644\u062a\u0631\u0628\u0629<\/td>Water and soil chemistry<\/td>2<\/td>2<\/td>CH-701<\/td><\/td>\n<\/tr>\n
3<\/td>CH \u2013 831<\/td>\u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0643\u0647\u0631\u0628\u064a\u0629 \u0627\u0644\u0645\u062a\u0642\u062f\u0645\u0629<\/td>Advanced \u00a0Electro analy. chemistry<\/td>2<\/td>2<\/td>CH-501<\/td><\/td>\n<\/tr>\n
4<\/td>CH \u2013 841<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u062a\u062d\u0644\u064a\u0644\u064a\u0629 \u0645\u062a\u0642\u062f\u0645\u0629<\/td>Advanced Analytical Chemistry<\/td>2<\/td>2<\/td>---<\/td><\/td>\n<\/tr>\n
5<\/td>CH \u2013 802<\/td>\u0646\u0638\u0631\u064a\u0629 \u0627\u0644\u0645\u062c\u0645\u0648\u0639\u0627\u062a<\/td>Group Theory in Chemistry<\/td>2<\/td>2<\/td>CH-502<\/td><\/td>\n<\/tr>\n
6<\/td>CH \u2013 822<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u063a\u064a\u0631 \u0639\u0636\u0648\u064a\u0629 \u0645\u062a\u0642\u062f\u0645\u0629<\/td>Advanced Inorganic Chemistry - I<\/td>2<\/td>2<\/td>CH-702<\/td><\/td>\n<\/tr>\n
7<\/td>CH \u2013 832<\/td>\u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0639\u0636\u0648\u064a\u0629 \u0627\u0644\u0645\u0639\u062f\u0646\u064a\u0629<\/td>Oregano Metallic Chemistry<\/td>2<\/td>2<\/td>CH-502<\/td><\/td>\n<\/tr>\n
8<\/td>CH \u2013 842<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u063a\u064a\u0631 \u0639\u0636\u0648\u064a\u0629 \u0645\u062a\u0642\u062f\u0645\u0629<\/td>Advanced Inorganic Chemistry - II<\/td>2<\/td>2<\/td>---<\/td><\/td>\n<\/tr>\n
9<\/td>CH \u2013 803<\/td>\u0627\u0644\u0635\u0628\u0627\u063a , \u0627\u0644\u0627\u0644\u064a\u0627\u0641 \u0648 \u0627\u0644\u0627\u0646\u0633\u062c\u0629<\/td>Dyes, Textile Fibers<\/td>2<\/td>2<\/td>CH-603<\/td><\/td>\n<\/tr>\n
10<\/td>CH \u2013 823<\/td>\u0643\u064a\u0645\u0627\u0621 \u0627\u0644\u0639\u0644\u0627\u062c\u064a\u0629 \u0648\u0627\u0644\u0641\u064a\u062a\u0627\u0645\u064a\u0646\u0627\u062a<\/td>Vitamins and Chemotherapy<\/td>2<\/td>2<\/td>CH-703<\/td><\/td>\n<\/tr>\n
11<\/td>CH \u2013 833<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0633\u0644\u064a\u0643\u0648\u0646 \u0648\u0627\u0644\u0645\u0631\u0643\u0628\u0627\u062a \u0627\u0644\u0639\u0636\u0648\u064a\u0629 \u0645\u062a\u0639\u062f\u062f\u0629 \u0627\u0644\u0627\u0646\u0648\u064a\u0629<\/td>Silicon Chemistry and Polynuclear Hydrocarbons<\/td>2<\/td>2<\/td>CH-703<\/td><\/td>\n<\/tr>\n
12<\/td>CH \u2013 843<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0639\u0636\u0648\u064a\u0629 \u0645\u062a\u0642\u062f\u0645\u0629<\/td>Advanced organic Chemistry<\/td>2<\/td>2<\/td>---<\/td><\/td>\n<\/tr>\n
13<\/td>CH \u2013 804<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0628\u0644\u0648\u0631\u0627\u062a \u0627\u0644\u0633\u0627\u0626\u0644\u0629<\/td>Liquid Crystals<\/td>2<\/td>2<\/td>CH-704<\/td><\/td>\n<\/tr>\n
14<\/td>CH \u2013 824<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0633\u0637\u0648\u062d \u0648\u0627\u0644\u0645\u062d\u0641\u0632\u0627\u062a<\/td>Surface Chemistry & Catalysis<\/td>2<\/td>2<\/td>CH-704<\/td><\/td>\n<\/tr>\n
15<\/td>CH \u2013 834<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u063a\u0631\u0648\u064a\u0627\u062a<\/td>Chemistry of Colloidal State<\/td>2<\/td>2<\/td>CH-304<\/td><\/td>\n<\/tr>\n
16<\/td>CH \u2013 844<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0641\u064a\u0632\u064a\u0627\u0626\u064a\u0629 \u0627\u0644\u0645\u062a\u0642\u062f\u0645\u0629<\/td>Advanced Physical Chemistry<\/td>2<\/td>2<\/td>---<\/td><\/td>\n<\/tr>\n
17<\/td>CH \u2013 820<\/td>\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0628\u064a\u0626\u0629 \u0648\u0627\u0644\u062a\u0644\u0648\u062b<\/td>Envor. Chemistry and pollution<\/td>2<\/td>2<\/td>---<\/td><\/td>\n<\/tr>\n
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\u0627\u0644\u0645\u062c\u0645\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0640\u0648\u0639<\/td><\/td><\/td><\/td>6<\/td><\/td><\/td><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n\n

\u062b\u0627\u0646\u064a\u0627: \u0645\u0631\u062d\u0644\u0629 \u0627\u0644\u062f\u0631\u0627\u0633\u0627\u062a \u0627\u0644\u0639\u0644\u064a\u0627\u00a0<\/strong><\/h3>\n

\u062f\u0631\u0627\u0633\u0627\u062a \u0627\u0644\u0639\u0644\u064a\u0627 \u0642\u0633\u0645 \u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0643\u0644\u064a\u0629 \u0627\u0644\u0639\u0644\u0648\u0645 \u062c\u0627\u0645\u0639\u0629 \u0633\u0628\u0647\u0627.csv<\/h2>\n\n\n\n\n\t\n\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t
I<\/th>M<\/th>Sc<\/th>Courses in Analytical Chemistry<\/th>\n<\/tr>\n<\/thead>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
1<\/td>Volumetric and Gravimetric Analysis (CH901-1\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
(Compulsory for all M<\/td>Sc<\/td>Students)<\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
Ionic equilibria, applications of volumetric analysis (neutralisation reactions, redox reactions, complexmetric reactions and precipitation reactions). Theory of gravimetric analysis. Microgravimetric and microvolumetric analysis. General introduction to separation in analytical chemistry. Masking and demasking agents. The analysis of real substances. Preliminary steps to an analysis.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
2<\/td>Instrumental Methods of Chemical Analysis I (CH901-2\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Instrumental methods of chemical analysis. Source of radiation(continuous sources-discrete sources). Optical materials(front surface mirror- reflection- filters and wavelength selection- gratings- prism- design of a dispersing system). Aspects of polarisation of light(selective absorption- selective reflection- anisotropic materials). Detectors(criteria for evaluation of detectors- photoelectric devices- photoemissive tube- photomultiperes- IR detectors). Monochromators and arrangements of optical components(prism systems spectrograph- UV spectrometers- IR spectrometers- grating mounts). Applications of UV visible, , IR spectroscopy.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
3<\/td>Instrumental Methods of Chemical Analysis II (CH901-3\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Atomic spectroscopy, atom population, selection rules, line profiles. Emission spectroscopy, flame emission, flame atomic absorption, atomic fluorescence. Intensity of spectral lines in absorption and emission. Measurement of line intensities by photographic procedures. Background connection. Applications of atomic absorption spectroscopy.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
4<\/td>Instrumental Methods of Chemical Analysis III (CH901-4\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
NMR spectroscopy; magnetic properties, nuclear energy level, resonance frequency, the NMR phenomena, instrumentation and techniques. Relaxation and line width, the chemical shift, measurement of chemical shift, spin-spin coupling, dianamic processes. Experimental aids to spectral analysis, lanthanide shift reagent, signal enhancement. Quantitative analysis.<\/td><\/td><\/td><\/td>\n<\/tr>\n
Mass spectrometry; principles of mass spectrometry design, determination of molecular weight, fragmentation, quantitative analysis, alternative ionisation techniques, analysis with GLC- MS interfacing systems, quadrapole mass spectrometry, mass spectrometry of involatile inorganic solids.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
5<\/td>Thermal and Radio Analysis (CH901-5\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Thermal methods of analysis; introduction to thermal analysis, thermogravimetry (TG), differential thermal analysis (DTA), thermometric titrations, miscellaneous thermal methods.<\/td><\/td><\/td><\/td>\n<\/tr>\n
Radiochemistry; revision of basics, decay rates and activity interaction of radiation, counting statistics, Gamma spectrometry, origin and nature of g radiation, interaction of g photons with matter, detection and measurement of g radiation, production of the spectrum, uses of spectra. Activation analysis, neutron activation analysis, isotope dilution analysis, liquid scintillation counting. The internal standard method, external standard method, channels ratio method, sample preparation. X-ray methods, origin of x-ray, apparatus, energy dispersive, x-ray emission spectroscopy, the x-ray fluorescence, x-ray and Auger photoelectron spectroscopy in analysis, solid state fluorescence spectroscopy, cantoluminescense spectroscopy, molecular emission cavity analysis. Molecular photoelectron spectroscopy using vacuum ultraviolet photons.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
6<\/td>Separation Techniques (CH901-6\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Analytical separations; separation by precipitation, extraction methods, applications of extraction procedures, ion exchange separation, separation of inorganic species by distillation. Chromatography; introduction to chromatography, classification of chromatography, paper chromatography, types of paper chromatography, experimental details for qualitative and quantitative analysis, application. Thin layer chromatography (TLC), superiority of TLC over other chromatographic techniques, experimental techniques, applications of TLC, limitations. Column chromatography, principle theory of development, experimental details, factors affecting column efficiency, applications of column chromatography. Gas chromatography, principles, instrumentation, evaluation, retention volume, resolution, applications. High performance liquid chromatography (HPLC), principles, instrumentation, applications. Electrophoresis, moving-boundary, curtain, zone and disk electrophoresis. Qualitative and quantitative analysis by chromatography.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
7<\/td>Electrochemical Analysis (CH901-7\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Electrochemical analysis, potentiometry, conductometry, high frequency titration, the measurement of pH, polarographic analysis, amperometric titration, electrolytic and coulometric techniques, electrogravimetry, polarimetry.<\/td><\/td><\/td><\/td>\n<\/tr>\n
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8<\/td>Environmental Chemistry (CH901-8\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Environmental chemistry and its scope, the nature composition of natural water, water pollution and trace level substance in water, water quality analysis and control, water treatment, environmental chemical analysis, industrial water analysis and control (water used in boilers, heat exchange, condensers), environmental chemistry of soil, the nature and composition of the atmosphere, particular matter and miner inorganic pollutants in the atmosphere, organic pollutants and photochemical smog in the atmosphere, natural resources and energy.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
9<\/td>Food Analysis (CH901-9\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Food analysis, analysis of dairy products, wheat, rice, meat products, soft drinks, preservatives, colouring matter and other additives.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
10<\/td>Seminars (CH901-10\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Review of articles and seminars<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
11<\/td>Special topics (CH901-16PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Theoretical and practical description of analytical materials<\/td><\/td><\/td><\/td>\n<\/tr>\n
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II<\/td>M<\/td>Sc<\/td>Courses in Inorganic Chemistry<\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
1<\/td>Coordination Chemistry of the Transition Metals (CH902-1\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
(Compulsory for all M<\/td>Sc<\/td>Students)<\/td><\/td>\n<\/tr>\n
Introduction and Nomenclature, coordination bonds (effective atomic number, VBT, CFT, MOT), isomerism, preparations and reactions of coordination compounds, complex ion stability, kinetics and mechanisms of reactions of coordination compounds<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
2<\/td>Spectroscopy (CH902-2\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Electronic transition spectroscopy, rotation-vibration spectroscopy, raman spectroscopy and IR spectra, nuclear magnetic resonance spectroscopy, magnetic properties of complexes, mass spectroscopy.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
3<\/td>Advanced Organometallic Chemistry (CH902-3\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Metal alkyl and aryl types: binuclear with metal-metal bond, polymeric with bridging alkyl groups, metalo-cyclic complexes, compounds with transition Metal carbon multiple bonds, metal compounds of heterocyclic (sandwich), 5 and 6 electron metal compounds, reactions of organometallic complexes (addition, oxidation, elimination, inserting). Metal carbonyl compounds (reactions and structures).<\/td><\/td><\/td><\/td>\n<\/tr>\n
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4<\/td>Nuclear and Radiation Chemistry (CH902-4\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Chemistry of lanthanides and octinides, nuclear particles (fundamental particles), kinds of radiation, radioactive atoms and radioactive series, radioactive Processes, measurement of radiation, uses of radioactive isotopes and radiation, nuclear reactors, atomic bomb.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
5<\/td>Chemical Application of Group Theory (CH902-5\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Symmetry operation and elements, rotation axes, reflection plane, inversion, rotation-reflection identity, symmetry groups (multiplying symmetry operation), systematic listing of symmetry groups (Cn , Cnn , Cnh , Dn , Dnh , Dnd , Sn , Td , Oc), molecular symmetry (coordination numbers 2, 3 , 4 , 5 , 6 , 7 , 8 , 9).<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
6<\/td>Representative of Non-transition Elements; (CH902-6\/PG (3 Credits)Bonding and Structures<\/td><\/td><\/td>\n<\/tr>\n
Electronic configuration (their ionization potential, radius, electron affinity, term Symbols, types of bonds: covalent, ionic, coordination, metallic, polar, hydrogen, hybridisation and structure (SP , SP2 , SP3 , SP3d , SP3d2 , dSP2 ), atomic covalent radii, van der waal radii, ionic radii, some relation between bond properties, bond order, length, force constant energy, halogens, interhalogens, noble gases.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
7<\/td>Industrial Inorganic Chemistry (CH902-7\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Bricks (40-60%, 10-25% Al2O3 ; 4-8% Fe2O3 ; 1-15% CaO), ceramics preparing and coloring), cement, sand stone and thrmoston from CaO, glass preparing and coloring (70-74% SiO2 ; 13-15% CaO ; 13-16% Na2O ), cells (dry cells, liquid cells), fertillizers (nitrogen and phosphate).<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
8<\/td>Bioinorganic Chemistry (CH902-8\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Most important inorganic elements for man kind, The pH of human body, chlorophyl a and b, ferredoxins and rubredoxins, hemoglobin and myoglobin (Protein), vitamin B12s [Co(III)] , and B12r [Co(II)], carboxy peptidase A (Zn), xanthine (Mo) and nitrogenage (Mo).<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
9<\/td>Seminars (CH902-9\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Review of articles and seminars<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
10<\/td>Special topics (CH902-17\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Theoretical and practical description of inorganic materials<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
III<\/td>M<\/td>Sc<\/td>Courses in Organic and Biochemistry<\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
1<\/td>Advanced Organic Chemistry (CH903-1\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
(Compulsory for all M<\/td>Sc<\/td>Students)<\/td><\/td>\n<\/tr>\n
Catalytic hydrogenation and dehydrogenation, metal hydride reductions and related reactions, dissolving metal reductions and relation reactions, reduction with hydrazine and its derivatives, oxidation with chromium and manganese compounds, oxidation with peracids and other peroxides, other methods of oxidation, halogenation, The alkylation of active methylene compounds, The aldol condensation and related reactions, acylation at carbon.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
2<\/td>Heterocyclic Chemistry (CH903-2\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Diazonaphthalenes (naphthyridines, benzodiazines, synthetic methods, chemical properties), purines and pteridines (syntheses and chemical properties), directed lithiation application to the synthesis of heterocyclic compounds, pyrylium salts and pyranones (natural synthesis, chemical properties), coumarines and chromones (synthesis and chemical properties), Flavones natural occurance, synthesis, chemical properties,a esters: versatile intermediates for the synthesis of polyaza-heterocycles, the carboniles and their compound, structure, natural occurance, synthesis and chemical properties, with more attention to their benzo derivatives, vicarious nucleophilic substitution of hydrogen (VMS): general review of nucleophilic substitution in aromatic compounds both carbocyclic and heterocyclic, VNS in general and its application to heterocycles compounds.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
3<\/td>The Conservation of Orbital Symmetry (CH903-3\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Orbitals and bonding, correlation diagrams, the conservation of orbital symmetry, the theory of electrocyclic reactions (electrocyclic reactions exemplified), the theory of cycloadditions and cycloreversion: (cycloadditions and cycloreversions exemplified, (2+2) cycloadditions in the photochemistry of the cyclohexadienones and cyclobexenones, The (2+2+2) cycloadditions, prismane, (2+2+2+2) cycloadditions), theory of sigmatropic reactions (sigmatropic reaction examplified, sequential sigmatropic shjfts), group transfers and eliminations, secondary effects, divertissements, cheletropic reactions, cyclo addition reactions of ketens, generalized selection rules for pericyclic reactions, violations.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
4<\/td>Chemistry of Natural Products (CH903-4\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Terpenoids, Carotenoids, Steroids and Alkaloids.<\/td><\/td><\/td><\/td>\n<\/tr>\n
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5<\/td>Optical Course (CH903-5\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
1- Carbohydrates, biochemistry an overview, monosaccharides, D-L faniles, disaccharides\/polysaccharides. Metabolism of Carbohydrates, respiratory chain phosphorylation and the chemiometic theory, Citric acid cycle and energy of living.<\/td><\/td><\/td><\/td>\n<\/tr>\n
2- Type of libides, chemical properties of triacqlglyerol, phospholipids, steroids, cell membranes, Metabolism of lipides, catabolism of fatty acids, anabolism of lipides and ketoacidosis and diabetes.<\/td><\/td><\/td><\/td>\n<\/tr>\n
3- Proteins, amino acids as blocks of proteins, primary structures of proteins, secondary structures of proteins, tertiary and quarternary proteins, common proteins pro\u00adperties, class of protein metabolism of amino acids, important of protein to energy cycles.<\/td><\/td><\/td><\/td>\n<\/tr>\n
4- Nucleic acids, nucleasides, structure of DNA, types of RNA, application of molecular biology protein bio-synthesis with ribonucleic acids, biological function of DNA, metabolism of ribo- and deoxy-ribonucleotides.<\/td><\/td><\/td><\/td>\n<\/tr>\n
5- Enzymes, regulations of ensymes, harmones and neurotransmiteas.<\/td><\/td><\/td><\/td>\n<\/tr>\n
6- Nutrition, general requirement, protein, vitamin, mineral and trace element.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
6<\/td>Organic Spectroscopy (CH903-6\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
energy and electromagnetic spectrum : the electromagnetic spectrum, absorption of electromagnetic radiat\u00adion by organic molecules; infra-red spectroscopy: units of frequency, wave length and wave number, molecular vibrations, calculation of vibrational frequency, modes of vibration, quantum restrictions, Factors influencing vibrational frequencies, sampling techniques, identification of functional groups by interpretation of infra-red spectra; nuclear magnetic resonance spectroscopy: the spinning.nucleus, the effect of an external magnetic field, precessional motion and precessional frequency, energy transitions, theory of NMR, chemical shift and its measurements, factors influencing chemical shift. electronegativity-shielding and deshielding, anisotropic effect, the splitting of NMR signals, theory of spin-spin splitting, coupling constant J . Proton exchange reactions, factors influencing geminal and vicinal coupling, long range coupling. non-first order spectra, identification of proton system by interpretation of NMR spectra; ultra-violet and visible spectroscopy: of electronic spectroscopy to conjugated dienes. unsaturated carbonyl compounds. Benzene and its substitution derivatives; Mass Spectroscopy: basic principles, the mass spectrometer, sample insertion, inlet system, ion production in the ionization chamber, separation of the ions in the analyzer, ions collections, isotope abundance, the molecular ion. metastable ions, fragmentation processes, fragmentations associated with functional groups.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
7<\/td>Physio-Organic Chemistry (CH903-7\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Energy of Activation, molecular orbitals, orbital symmetry, effects of structure on reactivity, rate of reaction: kinetics, first order ad second order reactions, mechanisms and methods of determining them, oxidation and reduction (mechanisms and reactions).<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
8<\/td>Stereochemistry (An Advanced Course ) (CH903-8\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 1<\/td>Optical and Geometrical Isomerism<\/td><\/td><\/td>\n<\/tr>\n
A. Optical Isomerism: polarimetry, molecular dissymmetry, Molecular Models.<\/td><\/td><\/td><\/td>\n<\/tr>\n
B<\/td>Optical Isomerism due to asymmetric carbon atom: compounds with on<\/td><\/td><\/td>\n<\/tr>\n
asymmetric carbon atom, compounds with two or more asymmetric carbon<\/td><\/td><\/td><\/td>\n<\/tr>\n
atom, compounds containing like asymmetric carbon atom in branched chain.<\/td><\/td><\/td><\/td>\n<\/tr>\n
C. Racemic modifications: nature of racemic modifications, formation of racemic modifications (by mixing, by synthesis, by racemisation), thermal Racemzations (by anion formation, by cation formation, by reversible formation of stable inactive intermediates, by walden inversion, by chemical Transfomation). Epimerization: (Mutarotation and first order asymmetric transformation, properties of racemic modification ( racemic mixtures, racemic compounds and racemic solid solutions)<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
9<\/td>General Topics (CH903-9\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Theoretical description of organic molecules: introduction to molecular orbital theory, hukel molecular orbital theory, the perturbational molecular orbital theory, the valence bond and resonance methods.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
10<\/td>Reactive Intermediates (CH903-10\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Isolation of intermediates, tapping of intermediates, alternative source of intermediates, kinetic evidence for reactive intermediates, some common types of reactive intermediates.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
11<\/td>Carbohydrates (CH903-11\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Carbohydrate Metabolism, review of CHO chemistry, glycolysis, glycogen synthesis, gluconeogensis, control of blood glucose, pentose phosphate pathway, uronic acid pathway, citric acid cycle, respiratory chain, alanine glucose cycle.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
12<\/td>Proteins and amino Acids Chemistry (CH903-12\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Protein and Amino acid Metabolism: review of protein and amino acid chemistry, classification of amino acids, classification of protein, protein function, biosynthesis of non-essential amino acids, catabolism of amino acids, amino acid nitrogen, amino acid carbon skeleton, conversion of amino acids to specialized products.<\/td><\/td><\/td><\/td>\n<\/tr>\n
13<\/td>Nucliec Acids (CH903-13\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Nucleotides and Nucleic acids: review of purines and pyrimidines chemistry, structure of DNA, structure of RNA, metabolism of purines and pyrimidines nucleotides, DNA organization and replication, RNA synthesis processing and metabolism, genetic code and protein synthesis, regulation of gene expression, recombinant DNA technology, cancer gene and growth factors.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
14<\/td>Fatty Acids (CH903-14\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Lipid Metaboism, review o f lipid chemistry, biosynthesis of fatty acids, oxidation of fatty acids, ketogensis, metabolism of unsaturated fatty acids, metabolism of acylglycerols, metabolism of sphingolipids, metabolism of cholestrol.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
15<\/td>Seminars (CH903-15\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Review of articles and seminars<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
16<\/td>Special topics (CH903-18\/PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Theoretical and practical description of organic materials<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
IV<\/td>M<\/td>Sc<\/td>Courses in Physical Chemistry<\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
1<\/td>Thermodynamics of non-ideal systems and statistical Thermodynamics (CH904\/1PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
(Compulsory for all M<\/td>Sc<\/td>Students)<\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
The chemical potential and escaping tendency - Equilibrium between two or more phases - The Fugacity - Standard free-energy functions and equilibrium calculations \u2013 Solutions - Non-electrolyte solutions - electrolyte solutions - Theories of electrolyte solutions - Thermal properties of solutions - Activity coefficient from solid - Liquid equilibria<\/td><\/td><\/td><\/td>\n<\/tr>\n
The distribution laws - Some more discussion of partition function - Thermodynamic functions in terms of the partition function - The molecular interpretation of the basic laws of thermodynamics - Evaluation of the partition function \u2013 Translational - Rotational, Vibrational, Electronic and Nuclear - Partition functions - Statistical thermodynamics of an ideal crystal - Ideal lattice gas, Statistical derivation of the equation of state for non-ideal fluids.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
2<\/td>Chemical Kinetics (CH904\/2PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Order of reaction - Rate constant - Complex reactions (reversible, consecutive and chain reactions) - Effect of temperature on reaction rate - Collision and transition state theories - Fast reactions in solutions (flow and relaxation methods),Statistical thermodynamics - Kinetics of acid-Base catalysis - Diffusion controlled elementary steps of solution reactions - Estimation of reaction from thermodynamic data - Photochemistry.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
3. Quantum Chemistry and Molecular structure (CH 904\/ 3 PG) (3 Credits) Quantum theory, quantum Mechanical Harmonic oscillator, molecular electronic structure, the Schr\u00f6dinger Wave Equation, molecular orbital description of the hydrogen molecule, electronic structure of polyatomic molecules, symmetry elements and symmetry operations, identification of point groups of molecules, rotational and vibrational spectroscopy, statistical mechanics.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
4<\/td>Spectroscopy (CH 904\/ 4 PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Electromagnetic radiation - Units, Regions of the spectrum, Line width, Resolution - Intensity - Selection Rules - Signal to Noise ratio - Absorption and Emission, Microwave - Infra-Red - Electronic and NMR spectroscopy - Electron Spin Resonance (ESR) spectroscopy - Fluorescence and Phosphorescence - Lasers, Mosbauer spectroscopy - Mass spectroscopy - Physical properties of Molecules: Dipole moment - Optical properties and magnetic properties.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
5. Electrochemistry (CH 904\/ 5 PG) (3 Credits) Kinetics of some electrode processes: the hydrogen evolution reaction at metal interfaces, the oxygen evolution reaction: the electrochemical oxidation and reduction: electrodepositing of metals and alloys, electrochemical dissolution and passivity of metals, electrochemical corrosion of metals:<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
6<\/td>Physical Chemistry of Polymers (CH 904\/ 6 PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
The kinetics of free radical polymerization - Copolymerization, <\/td><\/td><\/td><\/td>\n<\/tr>\n
Emulsion polymerization & ionic polymerization - The structure of vinyl polymers, Determination of molecular weights - molecular weight distribution in linear and non linear polymers - Configuration of polymer chains - Rubber elasticity- <\/td><\/td><\/td><\/td>\n<\/tr>\n
Statistical thermodynamics of polymer solutions - Phase equilibria in polymer Systems - configuration and frictional properties of the polymer molecule in dilute solution<\/td><\/td><\/td><\/td>\n<\/tr>\n
7<\/td>Surface Chemistry (CH 904\/ 7 PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
introduction and thermodynamics of adsorption, the physical and chemical adsorption of gases, treatment of solid adsorbent and gas adsorbed before adsorption. the use of gas or vapor for determination of surface area and pore size distribution, experimental techniques for studying the Gas-Solid Interface, the types of adsorption-desorption (sorption) isotherms, the physical sorption of gases by porous and nonporous solids, treatment of BET equation for adsorption isotherms, assessment of Porosity, the special behavior of water.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
8. Homogenous and Heterogeneous Catalysis (CH 904\/ 8 PG) (3 Credits) basic principles of catalysis, homogenous catalysts: structure, preparation and use, heterogeneous catalysts: structure, preparation and use, poisons and acceleration of catalysts, kinetics of catalyzed reaction, quantities aspects of catalysis by metals, catalysis in energy conversion, catalysis in the heavy inorganic chemical industry, application of Catalysis.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
9. Colloids: Chemistry of colloidal State (CH 904\/ 9 PG) (3 Credits) The nature of colloidal state, the different types of colloidal solutions, preparation of colloidal solutions, purification of colloidal solutions, collegative properties of colloidal solutions, sources of charges for the colloid Particles, the important application of colloids.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
10<\/td>Liquid Crystals (CH 904\/ 10 PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
What are liquid crystals (LCS) \u2013 thermotropic and lyotropic LCS, nematic, smectic and cholosteric, discotic phases; director and order-parameter - Liquid crystalline materials and properties - characterization of liquid crystalline phases - electronic properties of liquid crystals - Transport phenomena - Optical properties of liquid crystals. Theories of Liquid Crystal Displays (LCD) & photonic applications, operation of twisted nematic display - nonlinear optical properties of LCs. electro optical Properties of LCs. liquid crystal polymers (LCP) polymeric liquid phase transitions in liquid crystals. <\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
11<\/td>\u00a0 Photochemistry and Photobiology (CH 904\/ 11 PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
Introduction, thermal versus photochemical reactions, earth\u2019s atmosphere, the greenhouse effect, photochemical smog, the essential role of ozone in the stratosphere, photosynthesis I and II, mechanism of Vision, biological effects of radiation, problems.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
12<\/td>\u00a0 Environmental Chemistry and Catalysis in Atmospheric Pollution Control (CH 904\/ 12 PG) (3 Credits)<\/td><\/td><\/td>\n<\/tr>\n
overview for environmental chemistry, natural environmental pollution, human environmental pollution, treatment and disposal of chemical wastes, control of air pollution, the Role of catalysis in atmospheric pollution control.<\/td><\/td><\/td><\/td>\n<\/tr>\n
<\/td><\/td><\/td><\/td>\n<\/tr>\n
Electrolyte and Nonelectrolyte Solutions (CH 904\/ 13 PG) (3 Credits) Electrical conduction in solution, a molecular view of the solution process, thermodynamics of ions in solution, ionic activity, colligative properties of electrolyte and nonelectrolyte solutions, biological membranes, partial molar quantities, the thermodynamics of mixing, Binary Mixtures of Volatile Liquids, real solution<\/td><\/td><\/td><\/td>\n<\/tr>\n
\u0623<\/td><\/td><\/td><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n","protected":false},"excerpt":{"rendered":"

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