SELECT * FROM question_mgmt as q WHERE id=1992 AND status=1 SELECT id,question_no,question,chapter FROM question_mgmt as q WHERE courseId=3 AND subId=9 AND chapterId=66 and ex_no='1' AND status=1 ORDER BY CAST(question_no AS UNSIGNED)
Ortho and para nitrophenols are more acidic than phenol. Draw the resonance structures of the corresponding phenoxide ions.
Resonance structure of the phenoxide ion
Resonance structures of p-nitrophenoxide ion
Resonance structures of o-nitrophenoxide ion
It can be observed that the presence of nitro groups increases the stability of phenoxide ion.
The following results have been obtained during the kinetic studies of the reaction: 2A + B → C + D
Experiment |
A/ mol L - 1 |
B/ mol L - 1 |
Initial rate of formation of D/mol L - 1 min - 1 |
I | 0.1 | 0.1 |
6.0 × 10 - 3 |
II | 0.3 | 0.2 |
7.2 × 10 - 2 |
III | 0.3 | 0.4 |
2.88 × 10 - 1 |
IV | 0.4 | 0.1 |
2.40 × 10 - 2 |
Determine the rate law and the rate constant for the reaction.
Vapour pressure of pure acetone and chloroform at 328 K are 741.8 mm Hg and 632.8 mm Hg respectively. Assuming that they form ideal solution over the entire range of composition, plot ptotal' pchloroform' and pacetoneas a function of xacetone. The experimental data observed for different compositions of mixture is.
100 ×xacetone |
0 | 11.8 | 23.4 | 36.0 | 50.8 | 58.2 | 64.5 | 72.1 |
pacetone /mm Hg |
0 | 54.9 | 110.1 | 202.4 | 322.7 | 405.9 | 454.1 | 521.1 |
pchloroform/mm Hg |
632.8 | 548.1 | 469.4 | 359.7 | 257.7 | 193.6 | 161.2 | 120.7 |
Comments
Taking Screenshots on your Samsung Galaxy M31s is very easy and quick.
Report a problem on Specifications:
Taking Screenshots on your Samsung Galaxy M31s is very easy and quick.
Report a problem on Specifications:
Taking Screenshots on your Samsung Galaxy M31s is very easy and quick.
Report a problem on Specifications: