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Benzyl chloride undergoes SN1 reaction faster …

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Benzyl chloride undergoes SN1 reaction faster than cyclohexyl methyl chloride give reason..

Posted by Priya Dharshini ? 5 years, 11 months ago

CBSE > Class 12 > Chemistry

5 answers

Khuskaran Sidhu 5 years, 11 months ago

It forms resonance stablised carbocation while clorohexyl..... Do not

Řøhăň Řąjpůť ✌️✊ 5 years, 11 months ago

Benzyl chloride will undergo Sn1 reaction faster becoz it can form stable 2° carbocation which can be stabilized by π electrons of benzene ring. on the other hand in case of cyclohexyl methyl chloride, 1° carbocation is formed which is least stable.

Rohit Patel 5 years, 11 months ago

In sn1 rxn the reactivity depends upon the stability of carbocation formed in the first step. Due to stable nature of 3° carbonation, the sn1 rxn is favoured by heavy (bulky) groups on the carbon atom attached to halogens. And the sn1 order is- benzyl> allyl> 3°>2°>1°> methyl halides.

Nishu Goyal 5 years, 11 months ago

Stability of carbocation dekho pata lag jaega

Yogita Ingle 5 years, 11 months ago

Benzyl chloride undergoes SN1 reaction faster than cyclhexyl chloride because in case of benzyl chloride, the carbocation formed after the loss of CL- is stablised by resonance, whereas , no such stabilization is possible in the carbonation obtained from cyclohexyl methyl chloride.

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