12. ALDEHYDES KETONES AND CARBOXYLIC ACIDS
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26608 An alkene of molecular formula \({C_9}{H_{18}}\) on ozonolysis gives \(2,2\) dimethyl propanal and \(2-\) butanon, then the alkene is

1 \(2, \,2,\, 4-\)trimethyl \(-3-\) hexene
2 \(2, \,2,\, 6-\) trimethyl\(-3-\) hexene
3 \(2,\,3,\, 4-\) trimethyl \(-2-\) hexene
4 \(2,\, 2,\, 4-\) trimethyl \(-2-\) hexene
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26609 When m-chlorobenzaldehyde is treated with \(50\%\) \(KOH\) solution, the product \((s)\) obtained is (are)

1 358-a2
2 358-b2
3 358-c2
4 358-d2
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26610 \(A\) and \(B\) in the following reactions are

1 358-a3
2 358-b3
3 358-c3
4 \(A = RR'C{H_2}CN,B = NaOH\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26611 Reduction of Aldehydes and Ketones to hydrocarbon take place in the presence of

1 \(Zn\) amalgam and \(HCl\) acid
2 \(Pd/BaS{O_4}\)
3 Anhydrous \(AlC{l_3}\)
4 \(Ni/Pt\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26608 An alkene of molecular formula \({C_9}{H_{18}}\) on ozonolysis gives \(2,2\) dimethyl propanal and \(2-\) butanon, then the alkene is

1 \(2, \,2,\, 4-\)trimethyl \(-3-\) hexene
2 \(2, \,2,\, 6-\) trimethyl\(-3-\) hexene
3 \(2,\,3,\, 4-\) trimethyl \(-2-\) hexene
4 \(2,\, 2,\, 4-\) trimethyl \(-2-\) hexene
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26609 When m-chlorobenzaldehyde is treated with \(50\%\) \(KOH\) solution, the product \((s)\) obtained is (are)

1 358-a2
2 358-b2
3 358-c2
4 358-d2
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26610 \(A\) and \(B\) in the following reactions are

1 358-a3
2 358-b3
3 358-c3
4 \(A = RR'C{H_2}CN,B = NaOH\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26611 Reduction of Aldehydes and Ketones to hydrocarbon take place in the presence of

1 \(Zn\) amalgam and \(HCl\) acid
2 \(Pd/BaS{O_4}\)
3 Anhydrous \(AlC{l_3}\)
4 \(Ni/Pt\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26608 An alkene of molecular formula \({C_9}{H_{18}}\) on ozonolysis gives \(2,2\) dimethyl propanal and \(2-\) butanon, then the alkene is

1 \(2, \,2,\, 4-\)trimethyl \(-3-\) hexene
2 \(2, \,2,\, 6-\) trimethyl\(-3-\) hexene
3 \(2,\,3,\, 4-\) trimethyl \(-2-\) hexene
4 \(2,\, 2,\, 4-\) trimethyl \(-2-\) hexene
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26609 When m-chlorobenzaldehyde is treated with \(50\%\) \(KOH\) solution, the product \((s)\) obtained is (are)

1 358-a2
2 358-b2
3 358-c2
4 358-d2
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26610 \(A\) and \(B\) in the following reactions are

1 358-a3
2 358-b3
3 358-c3
4 \(A = RR'C{H_2}CN,B = NaOH\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26611 Reduction of Aldehydes and Ketones to hydrocarbon take place in the presence of

1 \(Zn\) amalgam and \(HCl\) acid
2 \(Pd/BaS{O_4}\)
3 Anhydrous \(AlC{l_3}\)
4 \(Ni/Pt\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26608 An alkene of molecular formula \({C_9}{H_{18}}\) on ozonolysis gives \(2,2\) dimethyl propanal and \(2-\) butanon, then the alkene is

1 \(2, \,2,\, 4-\)trimethyl \(-3-\) hexene
2 \(2, \,2,\, 6-\) trimethyl\(-3-\) hexene
3 \(2,\,3,\, 4-\) trimethyl \(-2-\) hexene
4 \(2,\, 2,\, 4-\) trimethyl \(-2-\) hexene
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26609 When m-chlorobenzaldehyde is treated with \(50\%\) \(KOH\) solution, the product \((s)\) obtained is (are)

1 358-a2
2 358-b2
3 358-c2
4 358-d2
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26610 \(A\) and \(B\) in the following reactions are

1 358-a3
2 358-b3
3 358-c3
4 \(A = RR'C{H_2}CN,B = NaOH\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26611 Reduction of Aldehydes and Ketones to hydrocarbon take place in the presence of

1 \(Zn\) amalgam and \(HCl\) acid
2 \(Pd/BaS{O_4}\)
3 Anhydrous \(AlC{l_3}\)
4 \(Ni/Pt\)