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Question : 21
Total: 27
(i) Out of ( CH 3 ) 3 C − Br and ( CH 3 ) 3 C − I , which one is more reactive towards S N 1 and why?
(ii) Write the product formed when p-nitrochlorobenzene is heated with aqueousNaOH at 443 K followed by acidification.
(iii) Why dextro - and laevo - rotatory isomers of Butan-2-ol are difficult to separate by fractional distillation?
(ii) Write the product formed when p-nitrochlorobenzene is heated with aqueous
(iii) Why dextro - and laevo - rotatory isomers of Butan-2-ol are difficult to separate by fractional distillation?
Solution:
(i) Within a group, larger atoms are better nucleophiles. I − > Br − > Cl − > F − , therefore I − is better leaving group than Br − .
(ii)
The presence of an electron withdrawing group( − NO 2 ) at ortho- and para-positions increases the reactivity of haloarenes.
(ii)
The presence of an electron withdrawing group
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