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p-dichlorobenzene has higher melting point than those of ortho and meta isomers. Give reason. |
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Answer» Solution : When methyl bromide undergoes hydrolysis with aqueoous potassium hydroxide , Methyl alcohol is formed . `CH_3-Br+ KOH to CH_3-OH +KBr` This mechanism involves only ONE step . The NUCLEOPHILE OH- attack from the REAR side of the leaving group . A transition atate with partial formtion of C-OH bond and partial breaking f C+Br bond TAKES place simultaneously . The rate of the reaction depends both on the concentration of nucleophile as well as alkyl halide Hence , It is a second order reaction . In `S_n^2` reaction , complete inversion of configuration takes place . `R-OH+ SOCl_2 to R-Cl +SO_2 +HCl` Swart.s Reaction Due to SYMMETRY of para - isomers |
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