Question

Which of the compounds will react faster in SN1 reaction with the-OH ion? CH3-CH2-Cl or C6H5-CH2-Cl

Answer 1

Answer:C6H5CH2Cl

Explanation:

Because benzyl carbo cation is more stable

Answer 2

Answer:

hi

Explanation:

SN1 reaction proceeds forward by creation of a carbocation and the stability of carbocation is

tertiary>secondary>primary..

here we have an alkyl halid as well as an aryl halide

aryl carbocation is more stable due to resonance

therefore C6H5-CH2-Cl will react faster with sn1

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