Tertiary alkyl halide undergoes solvolysis in either acetic acid or in ethanol .
(a) What is the solvolysis product in each solvent
( b) In which solvent reaction is more rapid and why ?

Tertiary alkyl undergoes solvolysis in either acetic acid or in ethanol.What is the solvolysis product in each solvent?

Tertiary alkyl undergoes solvolysis in either acetic acid or in ethanol. In which solvent reaction is more rapid and why?

In SN^2 , solvolysis RX in which the solvent is a nucleophile, what is the order and molecularity of the reaction ?

In SN^2 , solvolysis RX in which the solvent is a nucleophile, what is the order and molecularity of the reaction ?

SN^2 reactions of alkyl halides is a bimolecular reaction which take place through formation of a transition state. The rate of reaction depends on the concentration of alkyl halide and nucleophile.The reaction is favoured by strong nucleophlie in polar aprotic solvents. In which of the following solvents SN^2 reaction is more favourable

Explain why alkyl halides undergo nucleopilic substitution reaction more easily as compared to aryl halides ?

Predict the compound which will undergo solvolysis (aqueous ethanol) more rapidly.

SN^2 reactions of alkyl halides is a bimolecular reaction which take place through formation of a transition state. The rate of reaction depends on the concentration of alkyl halide and nucleophile.The reaction is favoured by strong nucleophlie in polar aprotic solvents. In the transition state in the SN^2 reaction is represented as . The central carbon atom is

(a) Why do acyl chlorides undergo nucleophilic attack more readily than alkyl chlorides ? (b) What is hydroxamic acid test and which functional group is determined by this test ?