Out of ch3ch(ch3)ch2cl and ch3ch2ch(ch3)cl which is more reactive towards sn1 reaction and why
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generally SN1 reactions are given by alkyl halides.
in the first step of SN1 reaction Carbo cation is formed, among tertiary secondary and primary Carbo cations tertiary carbocation is more stable than secondary carbocation that is more stable than primary carbon cation.
show the reactivity order of different alkyl halides towards SN1 reactions is tertiary alkyl halides are more reactive than secondary alkyl halides that are in turn more reactive than primary alkyl halides.
in the first step of SN1 reaction Carbo cation is formed, among tertiary secondary and primary Carbo cations tertiary carbocation is more stable than secondary carbocation that is more stable than primary carbon cation.
show the reactivity order of different alkyl halides towards SN1 reactions is tertiary alkyl halides are more reactive than secondary alkyl halides that are in turn more reactive than primary alkyl halides.
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This is due to the stabilisation of carbocation by resonance, as it is a allylic carbonation
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