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प्रश्न
Assertion (A) : Nucleophilic substitution of iodoethane is easier than chloroethane.
Reason (R) : Bond enthalpy of C-I bond is less than that of C-Cl bond.
विकल्प
Both (A) and (R) are true and (R) is the correct explanation of (A).
Both (A) and (R) are true, but (R) is not the correct explanation of (A).
(A) is true, but (R) is false.
(A) is false, but (R) is true.
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उत्तर
Both (A) and (R) are true and (R) is the correct explanation of (A).
Explanation:
Iodine is a better leaving group than chlorine because of its larger size, it will be released at a higher rate in the presence of an incoming nucleophile.
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संबंधित प्रश्न
The order of reactivity of the given haloalkanes towards nucleophile is:
Most reactive halide towards SN1 reaction is ____________.
Which of the following is the correct order of decreasing SN2 reactivity?
Identify X and Y in the following sequence:
\[\ce{C2H5Br ->[X] Product ->[Y] C3H7NH2}\]
Assertion: KCN reacts with methyl chloride to give methyl isocyanide.
Reason: CN– is an ambident nucleophile.
Which one of the following compounds is more reactive towards SN1 reaction?
In which reaction mechanism carbocation is formed?
Retention of configuration is observed in ______.
Which one of the following chlorohydrocarbons readily undergoes solvolysis?
The compound that will undergo SN1 reaction with the fastest rate is:
