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

26603 The oxidation of benzyl chloride with lead nitrate gives

1 Benzyl alcohol
2 Benzoic acid
3 Benzaldehyde
4 \(p-\)chlorobenzaldehyde
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26604 \(R - CH = C{H_2} + CO + {H_2}\) \(\mathop {\xrightarrow{{{\text{High Temp}}}}}\limits_{{\text{High Pressure}}} RC{H_2}C{H_2}CHO.\)   The above reaction is

1 Mendius reaction
2 Oxo process
3 Sandorn's reaction
4 Stephen's reaction
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26605 Glycerol reacts with potassium bisulphate to produce

1 Allyl iodide
2 Allyl sulphate
3 Acryl aldehyde
4 Glycerol trisulphate
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26606 The reagent used in Gatterman Koch aldehyde synthesis is

1 \(Pb/BaS{O_4}\)
2 alkaline \(KMn{O_4}\)
3 acidic \(KMn{O_4}\)
4 \(CO + HCl\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26607 On reductive ozonolysis yields

1 \(6-\)oxoheptanal
2 \(6-\)oxoheptanoic acid
3 \(6-\)hydroxyheptanal
4 \(3-\)hydroxypentanal
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26603 The oxidation of benzyl chloride with lead nitrate gives

1 Benzyl alcohol
2 Benzoic acid
3 Benzaldehyde
4 \(p-\)chlorobenzaldehyde
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26604 \(R - CH = C{H_2} + CO + {H_2}\) \(\mathop {\xrightarrow{{{\text{High Temp}}}}}\limits_{{\text{High Pressure}}} RC{H_2}C{H_2}CHO.\)   The above reaction is

1 Mendius reaction
2 Oxo process
3 Sandorn's reaction
4 Stephen's reaction
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26605 Glycerol reacts with potassium bisulphate to produce

1 Allyl iodide
2 Allyl sulphate
3 Acryl aldehyde
4 Glycerol trisulphate
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26606 The reagent used in Gatterman Koch aldehyde synthesis is

1 \(Pb/BaS{O_4}\)
2 alkaline \(KMn{O_4}\)
3 acidic \(KMn{O_4}\)
4 \(CO + HCl\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26607 On reductive ozonolysis yields

1 \(6-\)oxoheptanal
2 \(6-\)oxoheptanoic acid
3 \(6-\)hydroxyheptanal
4 \(3-\)hydroxypentanal
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26603 The oxidation of benzyl chloride with lead nitrate gives

1 Benzyl alcohol
2 Benzoic acid
3 Benzaldehyde
4 \(p-\)chlorobenzaldehyde
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26604 \(R - CH = C{H_2} + CO + {H_2}\) \(\mathop {\xrightarrow{{{\text{High Temp}}}}}\limits_{{\text{High Pressure}}} RC{H_2}C{H_2}CHO.\)   The above reaction is

1 Mendius reaction
2 Oxo process
3 Sandorn's reaction
4 Stephen's reaction
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26605 Glycerol reacts with potassium bisulphate to produce

1 Allyl iodide
2 Allyl sulphate
3 Acryl aldehyde
4 Glycerol trisulphate
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26606 The reagent used in Gatterman Koch aldehyde synthesis is

1 \(Pb/BaS{O_4}\)
2 alkaline \(KMn{O_4}\)
3 acidic \(KMn{O_4}\)
4 \(CO + HCl\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26607 On reductive ozonolysis yields

1 \(6-\)oxoheptanal
2 \(6-\)oxoheptanoic acid
3 \(6-\)hydroxyheptanal
4 \(3-\)hydroxypentanal
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26603 The oxidation of benzyl chloride with lead nitrate gives

1 Benzyl alcohol
2 Benzoic acid
3 Benzaldehyde
4 \(p-\)chlorobenzaldehyde
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26604 \(R - CH = C{H_2} + CO + {H_2}\) \(\mathop {\xrightarrow{{{\text{High Temp}}}}}\limits_{{\text{High Pressure}}} RC{H_2}C{H_2}CHO.\)   The above reaction is

1 Mendius reaction
2 Oxo process
3 Sandorn's reaction
4 Stephen's reaction
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26605 Glycerol reacts with potassium bisulphate to produce

1 Allyl iodide
2 Allyl sulphate
3 Acryl aldehyde
4 Glycerol trisulphate
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26606 The reagent used in Gatterman Koch aldehyde synthesis is

1 \(Pb/BaS{O_4}\)
2 alkaline \(KMn{O_4}\)
3 acidic \(KMn{O_4}\)
4 \(CO + HCl\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26607 On reductive ozonolysis yields

1 \(6-\)oxoheptanal
2 \(6-\)oxoheptanoic acid
3 \(6-\)hydroxyheptanal
4 \(3-\)hydroxypentanal
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26603 The oxidation of benzyl chloride with lead nitrate gives

1 Benzyl alcohol
2 Benzoic acid
3 Benzaldehyde
4 \(p-\)chlorobenzaldehyde
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26604 \(R - CH = C{H_2} + CO + {H_2}\) \(\mathop {\xrightarrow{{{\text{High Temp}}}}}\limits_{{\text{High Pressure}}} RC{H_2}C{H_2}CHO.\)   The above reaction is

1 Mendius reaction
2 Oxo process
3 Sandorn's reaction
4 Stephen's reaction
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26605 Glycerol reacts with potassium bisulphate to produce

1 Allyl iodide
2 Allyl sulphate
3 Acryl aldehyde
4 Glycerol trisulphate
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26606 The reagent used in Gatterman Koch aldehyde synthesis is

1 \(Pb/BaS{O_4}\)
2 alkaline \(KMn{O_4}\)
3 acidic \(KMn{O_4}\)
4 \(CO + HCl\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

26607 On reductive ozonolysis yields

1 \(6-\)oxoheptanal
2 \(6-\)oxoheptanoic acid
3 \(6-\)hydroxyheptanal
4 \(3-\)hydroxypentanal