which type of atomic displacement reaction show by tertiary secondary and primary halides explain mechanism
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The elimination–ddition mechanism of aryl halides requires an amide ion, a very strong base, to abstract a proton from the position ortho to the halogen atom. An elimination reaction in occurs in which the halide ion is the leaving group. A very reactive intermediate called benzyne results.
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Explanation:
The elimination–ddition mechanism of aryl halides requires an amide ion, a very strong base, to abstract a proton from the position ortho to the halogen atom. An elimination reaction in occurs in which the halide ion is the leaving group. A very reactive intermediate called benzyne results.
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