One mole of an organic compound A with the formula C3H8O reacts completely with two moles of HI to form X and Y. When Y is boiled with aqueous alkali, it forms Z . Z answers the iodoform test. The compound A is
propan -2- ol
propan - 1- ol
ethoxyethane
methoxyethane
D.
methoxyethane
A compound (A) C4H8Cl2 on alkaline hydrolysis to give compound (B) C4H8O which gives an oxime and positive Tollen's reagent test. What is the structure of (A)?
CH3CH2CH2CHCl2
CH3CCl2CH2CH3
CH3CH(Cl)CH(Cl)CH3
CH2ClCH2CH2CH2Cl
The increasing order of the rate of HCN addition to compound A-D is
A. HCHO B. CH3COCH3
C.PhCOCH3 D. PhCOPh
A< B < C < D
D< B< C< A
D < C < B < A
C < D< B< A
If 'A' is C2H5NH2, 'B' is (C2H5)NH, 'C' is (C2H5)3N, then order of solubility in water is
A >B > C
B < A <C
C < B <A
C > B <A