26603
The oxidation of benzyl chloride with lead nitrate gives
1 Benzyl alcohol
2 Benzoic acid
3 Benzaldehyde
4 \(p-\)chlorobenzaldehyde
Explanation:
Benzoin is an organic compound with the formula \(PhCH ( OH ) COPh\). It is a hydroxy ketone attached to two phenyl groups. It is alpha hydroxy ketone.
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
Explanation:
when reaction between any alkene and water gas \(\left( CO + H _2\right)\) is occur at high tempereture and high pressure the product will be an aldehyde and this processis called oxo process.
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
Explanation:
Glycerol on heating potassium Bisulfate , undergoes dehydration with removal of two water molecule from the glycerol molecule. Hence, resulting in formation of unsaturated aldehyde i.e acrylic aldehyde.
ALDEHYDES, KETONES AND CARBOXYLIC ACID
26606
The reagent used in Gatterman Koch aldehyde synthesis is
26603
The oxidation of benzyl chloride with lead nitrate gives
1 Benzyl alcohol
2 Benzoic acid
3 Benzaldehyde
4 \(p-\)chlorobenzaldehyde
Explanation:
Benzoin is an organic compound with the formula \(PhCH ( OH ) COPh\). It is a hydroxy ketone attached to two phenyl groups. It is alpha hydroxy ketone.
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
Explanation:
when reaction between any alkene and water gas \(\left( CO + H _2\right)\) is occur at high tempereture and high pressure the product will be an aldehyde and this processis called oxo process.
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
Explanation:
Glycerol on heating potassium Bisulfate , undergoes dehydration with removal of two water molecule from the glycerol molecule. Hence, resulting in formation of unsaturated aldehyde i.e acrylic aldehyde.
ALDEHYDES, KETONES AND CARBOXYLIC ACID
26606
The reagent used in Gatterman Koch aldehyde synthesis is
26603
The oxidation of benzyl chloride with lead nitrate gives
1 Benzyl alcohol
2 Benzoic acid
3 Benzaldehyde
4 \(p-\)chlorobenzaldehyde
Explanation:
Benzoin is an organic compound with the formula \(PhCH ( OH ) COPh\). It is a hydroxy ketone attached to two phenyl groups. It is alpha hydroxy ketone.
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
Explanation:
when reaction between any alkene and water gas \(\left( CO + H _2\right)\) is occur at high tempereture and high pressure the product will be an aldehyde and this processis called oxo process.
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
Explanation:
Glycerol on heating potassium Bisulfate , undergoes dehydration with removal of two water molecule from the glycerol molecule. Hence, resulting in formation of unsaturated aldehyde i.e acrylic aldehyde.
ALDEHYDES, KETONES AND CARBOXYLIC ACID
26606
The reagent used in Gatterman Koch aldehyde synthesis is
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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
Explanation:
Benzoin is an organic compound with the formula \(PhCH ( OH ) COPh\). It is a hydroxy ketone attached to two phenyl groups. It is alpha hydroxy ketone.
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
Explanation:
when reaction between any alkene and water gas \(\left( CO + H _2\right)\) is occur at high tempereture and high pressure the product will be an aldehyde and this processis called oxo process.
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
Explanation:
Glycerol on heating potassium Bisulfate , undergoes dehydration with removal of two water molecule from the glycerol molecule. Hence, resulting in formation of unsaturated aldehyde i.e acrylic aldehyde.
ALDEHYDES, KETONES AND CARBOXYLIC ACID
26606
The reagent used in Gatterman Koch aldehyde synthesis is
26603
The oxidation of benzyl chloride with lead nitrate gives
1 Benzyl alcohol
2 Benzoic acid
3 Benzaldehyde
4 \(p-\)chlorobenzaldehyde
Explanation:
Benzoin is an organic compound with the formula \(PhCH ( OH ) COPh\). It is a hydroxy ketone attached to two phenyl groups. It is alpha hydroxy ketone.
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
Explanation:
when reaction between any alkene and water gas \(\left( CO + H _2\right)\) is occur at high tempereture and high pressure the product will be an aldehyde and this processis called oxo process.
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
Explanation:
Glycerol on heating potassium Bisulfate , undergoes dehydration with removal of two water molecule from the glycerol molecule. Hence, resulting in formation of unsaturated aldehyde i.e acrylic aldehyde.
ALDEHYDES, KETONES AND CARBOXYLIC ACID
26606
The reagent used in Gatterman Koch aldehyde synthesis is
