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Which of the following order is correct for the decreasing reactivity to ring monobromination of the following compounds? A. ` I gt II gt III gt IV`B. `I gt III gt II gt IV`C. `II gt III gt IV gt I`D. `III gt I gt III gt IV`

Answer» Correct Answer - B
Bromination of arenes is an electrophilic substitution reaction. The higher the electron density on the benzene ring, more is the ease with which the ring undergoes substitution. The presence of +R effect increases the reactivity while -R effect decreases it
`NO_(2)` is more deactivating than `-COOH` since N is +vely charged and withdraws more electrons form benzene than `-COOH`


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