
Decreasing order of acidity of the following terminal acetylenes is

- (i) \(>\) (iii) \(>\) (ii) \(>\) (iv)
- (i) \(>\) (ii) \(>\) (iv) \(>\) (iii)
- (i) \(>\) (iv) \(>\) (ii) \(>\) (iii)
- (i) \(>\) (iii) \(>\) (iv) \(>\) (ii)
Solution

EWG \((-R)\) stabilise carbanions but EDG \((+R > +I)\) destabilise carbanions. [EWG : Electron withdrawing group EDG : Electron donating group] A stronger acid produces stable conjugate base. So, the order of acidity will be \(\text { (i) } > \text { (ii) } > \text { (iv) } > \text { (iii) }\)
Asked in: AP EAMCET 2020 (17 Sep Shift 1)