Greater nucleophilicity is of
Do let me know if the answers are correct
Answer of 1 will be c-c-o(-) because nucleophilic strength is reverse of acidic strength.
Similarly order of 2 question will be 1>2.
Reason is same.
But I think in Q2 b>a because in 'a' nucleophilicity will be reduced due to steric hindrance
Lesser is the stability of -ve charge , more is it’s tendency to attack as a nucleophile
Yes 2 should be B.
Because nucleophilocity is kinetically controlled product and though negative chatge concentration increases but it is sterically hindered way too much comapred to other compound
For both 1 and 2 it should be B