CARBOXYLIC ACIDS
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28486 Which of the following compounds will form the precipitate with aq. AgNO\(_{3}\) solution most readily $?$

1 983-a112
2 983-b112
3 983-c112
4 983-d112
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28487 The decreasing order of reactivity of the following organic molecules towards \(AgNO\) \(_{3}\) solution is :

1 \(( A )>( B )>( D )>( C )\)
2 \(( A )>( B )>( C )>( D )\)
3 \((C)>(D)>(A)>(B)\)
4 \((B)>(A)>(C)>(D)\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28488 An organic compound \((A)\) (molecular formula \(\left. C _{6} H _{12} O _{2}\right)\) was hydrolysed with dil. \(H _{2} SO _{4}\) to give a carboxylic acid \((B)\) and an alcohol \((C).\) \('C'\) give white turbidity immediately when treated with anhydrous \(ZnCl _{2}\) and conc. \(HCl\). The organic compound \((A)\) is

1 983-a134
2 983-b134
3 983-c134
4 983-d134
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28489 \([ P ]\) on treatment with \(Br _{2} / FeBr _{3}\) in \(CCl _{4}\)produced a single isomer \(C _{8} H _{7} O _{2}\) \(Br\) while heating \([P]\) with sodalime gave toluene.The compound \([P]\) is :

1 983-a138
2 983-b138
3 983-c138
4 983-d138
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28486 Which of the following compounds will form the precipitate with aq. AgNO\(_{3}\) solution most readily $?$

1 983-a112
2 983-b112
3 983-c112
4 983-d112
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28487 The decreasing order of reactivity of the following organic molecules towards \(AgNO\) \(_{3}\) solution is :

1 \(( A )>( B )>( D )>( C )\)
2 \(( A )>( B )>( C )>( D )\)
3 \((C)>(D)>(A)>(B)\)
4 \((B)>(A)>(C)>(D)\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28488 An organic compound \((A)\) (molecular formula \(\left. C _{6} H _{12} O _{2}\right)\) was hydrolysed with dil. \(H _{2} SO _{4}\) to give a carboxylic acid \((B)\) and an alcohol \((C).\) \('C'\) give white turbidity immediately when treated with anhydrous \(ZnCl _{2}\) and conc. \(HCl\). The organic compound \((A)\) is

1 983-a134
2 983-b134
3 983-c134
4 983-d134
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28489 \([ P ]\) on treatment with \(Br _{2} / FeBr _{3}\) in \(CCl _{4}\)produced a single isomer \(C _{8} H _{7} O _{2}\) \(Br\) while heating \([P]\) with sodalime gave toluene.The compound \([P]\) is :

1 983-a138
2 983-b138
3 983-c138
4 983-d138
NEET Test Series from KOTA - 10 Papers In MS WORD WhatsApp Here
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28486 Which of the following compounds will form the precipitate with aq. AgNO\(_{3}\) solution most readily $?$

1 983-a112
2 983-b112
3 983-c112
4 983-d112
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28487 The decreasing order of reactivity of the following organic molecules towards \(AgNO\) \(_{3}\) solution is :

1 \(( A )>( B )>( D )>( C )\)
2 \(( A )>( B )>( C )>( D )\)
3 \((C)>(D)>(A)>(B)\)
4 \((B)>(A)>(C)>(D)\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28488 An organic compound \((A)\) (molecular formula \(\left. C _{6} H _{12} O _{2}\right)\) was hydrolysed with dil. \(H _{2} SO _{4}\) to give a carboxylic acid \((B)\) and an alcohol \((C).\) \('C'\) give white turbidity immediately when treated with anhydrous \(ZnCl _{2}\) and conc. \(HCl\). The organic compound \((A)\) is

1 983-a134
2 983-b134
3 983-c134
4 983-d134
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28489 \([ P ]\) on treatment with \(Br _{2} / FeBr _{3}\) in \(CCl _{4}\)produced a single isomer \(C _{8} H _{7} O _{2}\) \(Br\) while heating \([P]\) with sodalime gave toluene.The compound \([P]\) is :

1 983-a138
2 983-b138
3 983-c138
4 983-d138
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28486 Which of the following compounds will form the precipitate with aq. AgNO\(_{3}\) solution most readily $?$

1 983-a112
2 983-b112
3 983-c112
4 983-d112
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28487 The decreasing order of reactivity of the following organic molecules towards \(AgNO\) \(_{3}\) solution is :

1 \(( A )>( B )>( D )>( C )\)
2 \(( A )>( B )>( C )>( D )\)
3 \((C)>(D)>(A)>(B)\)
4 \((B)>(A)>(C)>(D)\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28488 An organic compound \((A)\) (molecular formula \(\left. C _{6} H _{12} O _{2}\right)\) was hydrolysed with dil. \(H _{2} SO _{4}\) to give a carboxylic acid \((B)\) and an alcohol \((C).\) \('C'\) give white turbidity immediately when treated with anhydrous \(ZnCl _{2}\) and conc. \(HCl\). The organic compound \((A)\) is

1 983-a134
2 983-b134
3 983-c134
4 983-d134
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28489 \([ P ]\) on treatment with \(Br _{2} / FeBr _{3}\) in \(CCl _{4}\)produced a single isomer \(C _{8} H _{7} O _{2}\) \(Br\) while heating \([P]\) with sodalime gave toluene.The compound \([P]\) is :

1 983-a138
2 983-b138
3 983-c138
4 983-d138