Journal of the American Chemical Society

4-PARA-TOLYLSEMICARBAZIDE AND CERTAIN DERIVATIVES1

AS Wheeler, RW Bost

Index: Wheeler; Bost Journal of the American Chemical Society, 1924 , vol. 46, p. 2814

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Citation Number: 2

Abstract

In certain cases where an aldehyde or ketone is particularly sensitive to alkaline reagents, semicarbazide and phenylsemicarbazide have a great advantage over hydroxylamine as reagents for the carbonyl group. There may be cases where phenylsemicarbazide has an advantage over semicarbazide on account of its increased negativity. Of the three known phenylsemicarbazides the 1-phenylsemicarbazide has not been employed. The 2- ...

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