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प्रश्न
Which would undergo SN2 reaction faster in the following pair and why ?
CH3 – CH2 – Br and CH3 – CH2 – I
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उत्तर
CH3 – CH2 – I would undergo an SN2 reaction faster than CH3 – CH2 – Br. Since iodine is a better leaving group because of its large size, it will be released at a faster rate in the presence of an incoming nucleophile as compared to bromine.
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संबंधित प्रश्न
Write the structure of an isomer of compound C4H9Br which is most reactive towards SN1 reaction
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\[\ce{CH3CH2Br + KCN ->[aq{.} ethanol]}\]
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(A) 2° > 3° > 1°
(B) 3° > 2° > 1°
(C) 3° > 1° > 2°
(D) 1° > 3° > 2°
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(i) The given reaction follows SN2 mechanism.
(ii) (b) and (d) have opposite configuration.
(iii) (b) and (d) have same configuration.
(iv) The given reaction follows SN1 mechanism.
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