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Bhamini
17 May 2016

An organic compound ‘A’ with molecular formula C6H7N, on treatment with NaNO2 + HCl at 273 − 278 K, gives an intermediate ‘B’ that reacts with cuprous chloride to form ‘C’. Compound ‘C’ reacts with methyl chloride in the presence of anhydrous AlCl3 to form ‘D’ and ‘E’. Among ‘D’ and ‘E’ the major product on treatment with sodium in dry ether forms compound ‘F’. Identify compounds A to F. Write the reactions involved.

OR

Complete the given reactions.

a.

b.

c.

or
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Butyl Bromide B Racemic Mixture Optically InactiveWould Undergo Sn2 Reaction Faster Following Pair Give Reasons N Butyl Bromide Higher Boiling Point Butyl Bromide B Racemic Mixture Optically InactiveWould Undergo Sn2 Reaction Faster Following Pair Give Reasons N Butyl Bromide Higher Boiling Point Butyl Bromide B Racemic Mixture Optically InactiveWould Undergo Sn1 Reaction Faster Following Pair Write Structure Major Product Following Reactions Give Reasons Following Phenol Acidic Ethanol Ii Boiling Point Ethanol Higher Comparison MethoxymethaWould Undergo Sn2 Reaction Faster Following Pair Ch3 Ch2 Br Ch3 Ch2 Alkyl Halides Insoluble Water B Butan 1 Ol Optically Inactive Butan 2 Ol Optically Active C AlthougPredict Products Following Reactions Ch3 Ch Ch2 Ii 3 H2o2 Oh B2h6 Ii C6h5 Oh Br2aq Iii Ch3ch2oh Cu 5Reactive Towards Sn1 Reaction Given Reasons C Cl Bond Length Chlorobenzene Shorter C Cl Bond Length Ch3 Cl Ii Dipole Moment ChloroWrite Structure Isomer Compound C4h9br Reactive Towards 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