Acidic Powers & Their Orders - Chemistry Fact Sheet- 1
Acidic Powers & Their Orders - Chemistry Fact Sheet- 1
1. | ![]() | Farther the (–I) group (Cl), lesser the acidic strength | |
2. | ![]() | Farther the (+I) group, greater the acidic power | |
3. | ![]() | —CH3 is electron donating and — NO2 is electron attracting | |
4. | ![]() | —CH3 is electron repelling; decreases acidic strength of phenol | |
5. | ![]() | — OCH3 group contains +M effect and decreases acidic poer. | |
6. | ![]() | — NO2 is electron attracting; III is more resonance stabilised than I and also than II. In I, only inductive effect is operative. | |
7. | ![]() | sp2 hybridised carbon of I, II are more el-ectronegative hence acid strength is inc-reased. Benzylic (C6H5CH2) is more stab-ilised than allylic (CH2==CHCH2). | |
8. | ![]() | Effect of one —COOH on the other decr-eases as its distance between them increases, (COOH)2 is maximum acidic. | |
9. | ![]() | —NO2 is electron attracting (–I effect) | |
10. | ![]() | —OH shows electron withdrawing nature at o - and m - and electron repelling at p -, o - isomer due to intramolecular bonding in salicylate ion is stronger than m - isomer | |
11. | ![]() | —do— | |
12. | ![]() | —NH2 is electron donating. |