A compound x c2h4o on oxidation gives y c2h4o2 . X undergoes haloform reaction. On treatment with hcn,
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An organic compound A (C8H10O) neither gives tollen's test nor gives iodoform test. (A) on treatment with HBr with An yields hydrocarbon (D) which burns with sooty flame. Compound (C) forms analkene on treatment with alcohol KOH . Identify A,B,C,D and write reaction involved.
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Answer:
Explanation:
1)x=CH3CHO
y=CH3COOH
2)CH3CHO + NaOH -----> CH3CHOHCH2CHO (Aldol Reaction)
the product is 3- hydroxy butanaldehyde
3)
CH3CHO+ KMnO4 -----------> CH3COOH
CH3CHO + NaOH + I2 -----> CH3CHOH + CHI3
CH3CHO + HCN --------> CH3CHOHCN (Z)
CH3CHOHCN + H2O ------> CH3CHOHCOOH
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