The reaction of with aqueous sodium hydroxide follows:
1. | S1mechanism |
2. | S2 mechanism |
3. | Any of the above is depending upon the temperature of the reaction. |
4. | Saytzetf rule |
carbocation will increase, the rate and possibility of SN1 mechanism will increase. For the given substrate since stable carbocation is involved, Hence mechanism of reaction is SN1. Here this benzyl carbocation is stabilized by resonance of benzene ring double bonds.
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