323625
Oxidation of acetaldehyde with selenium dioxide produces
1 ethanoic acid
2 methanoic acid
3 glyoxal
4 oxalic acid
Explanation:
Selenium dioxide oxidises aldehydes and ketones at \({\rm{\alpha }}\)-position to carbonyl group. \({\text{C}}{{\text{H}}_{\text{3}}}{\text{CHO}} \to \mathop {{\text{OHC}}.{\text{CHO}}}\limits_{{\text{Glyoxal}}} \)
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS
323626
\({\text{3C}}{{\text{H}}_{\text{3}}}{\text{CHO}}\xrightarrow[{{\text{298\;K}}}]{{{{\text{H}}^{\text{ + }}}}}{\text{A}}\). Product ' \(\mathrm{A}\) ' is a pleasant smelling liquid (B.P. \(=410 \mathrm{~K})\). It is used as a/an
1 Explosive
2 Hypnotic
3 Tear gas
4 Solvent
Explanation:
A =
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS
323627
Which of the following substances does not give \(\mathrm{HCHO}\) on heating or distillation?
1 Paraformaldehyde
2 Formalin
3 Paraldehyde
4 Trioxane
Explanation:
Paraldehyde is a derivative of \(\mathrm{CH}_{3} \mathrm{CHO}\)
323625
Oxidation of acetaldehyde with selenium dioxide produces
1 ethanoic acid
2 methanoic acid
3 glyoxal
4 oxalic acid
Explanation:
Selenium dioxide oxidises aldehydes and ketones at \({\rm{\alpha }}\)-position to carbonyl group. \({\text{C}}{{\text{H}}_{\text{3}}}{\text{CHO}} \to \mathop {{\text{OHC}}.{\text{CHO}}}\limits_{{\text{Glyoxal}}} \)
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS
323626
\({\text{3C}}{{\text{H}}_{\text{3}}}{\text{CHO}}\xrightarrow[{{\text{298\;K}}}]{{{{\text{H}}^{\text{ + }}}}}{\text{A}}\). Product ' \(\mathrm{A}\) ' is a pleasant smelling liquid (B.P. \(=410 \mathrm{~K})\). It is used as a/an
1 Explosive
2 Hypnotic
3 Tear gas
4 Solvent
Explanation:
A =
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS
323627
Which of the following substances does not give \(\mathrm{HCHO}\) on heating or distillation?
1 Paraformaldehyde
2 Formalin
3 Paraldehyde
4 Trioxane
Explanation:
Paraldehyde is a derivative of \(\mathrm{CH}_{3} \mathrm{CHO}\)
323625
Oxidation of acetaldehyde with selenium dioxide produces
1 ethanoic acid
2 methanoic acid
3 glyoxal
4 oxalic acid
Explanation:
Selenium dioxide oxidises aldehydes and ketones at \({\rm{\alpha }}\)-position to carbonyl group. \({\text{C}}{{\text{H}}_{\text{3}}}{\text{CHO}} \to \mathop {{\text{OHC}}.{\text{CHO}}}\limits_{{\text{Glyoxal}}} \)
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS
323626
\({\text{3C}}{{\text{H}}_{\text{3}}}{\text{CHO}}\xrightarrow[{{\text{298\;K}}}]{{{{\text{H}}^{\text{ + }}}}}{\text{A}}\). Product ' \(\mathrm{A}\) ' is a pleasant smelling liquid (B.P. \(=410 \mathrm{~K})\). It is used as a/an
1 Explosive
2 Hypnotic
3 Tear gas
4 Solvent
Explanation:
A =
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS
323627
Which of the following substances does not give \(\mathrm{HCHO}\) on heating or distillation?
1 Paraformaldehyde
2 Formalin
3 Paraldehyde
4 Trioxane
Explanation:
Paraldehyde is a derivative of \(\mathrm{CH}_{3} \mathrm{CHO}\)
323625
Oxidation of acetaldehyde with selenium dioxide produces
1 ethanoic acid
2 methanoic acid
3 glyoxal
4 oxalic acid
Explanation:
Selenium dioxide oxidises aldehydes and ketones at \({\rm{\alpha }}\)-position to carbonyl group. \({\text{C}}{{\text{H}}_{\text{3}}}{\text{CHO}} \to \mathop {{\text{OHC}}.{\text{CHO}}}\limits_{{\text{Glyoxal}}} \)
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS
323626
\({\text{3C}}{{\text{H}}_{\text{3}}}{\text{CHO}}\xrightarrow[{{\text{298\;K}}}]{{{{\text{H}}^{\text{ + }}}}}{\text{A}}\). Product ' \(\mathrm{A}\) ' is a pleasant smelling liquid (B.P. \(=410 \mathrm{~K})\). It is used as a/an
1 Explosive
2 Hypnotic
3 Tear gas
4 Solvent
Explanation:
A =
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS
323627
Which of the following substances does not give \(\mathrm{HCHO}\) on heating or distillation?
1 Paraformaldehyde
2 Formalin
3 Paraldehyde
4 Trioxane
Explanation:
Paraldehyde is a derivative of \(\mathrm{CH}_{3} \mathrm{CHO}\)