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प्रश्न
What product will be formed on reaction of propanal with 2-methylpropanal in the presence of \[\ce{NaOH}\]? What products will be formed? Write the name of the reaction also.
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उत्तर
It is cross Aldol condensation
\[\begin{array}{cc}
\phantom{}\ce{CH3}\phantom{.................}\ce{OH}\phantom{...............}\ce{CH3}\phantom{..........}\ce{CH3}\phantom{............}\ce{CH3}\phantom{.}\ce{OH}\phantom{...}\ce{CH3}\phantom{....}\ce{H3C}\phantom{...}\\
\phantom{}|\phantom{....................}|\phantom{..................}|\phantom{.............}|\phantom{................}|\phantom{....}|\phantom{......}|\phantom{...........}\backslash\phantom{.}\\
\phantom{}\ce{CH3CH2CHO + CH3CHCH3 -> CH3CH2CH - C - CHO + CH2 - CH = C - CHO + CH3C - CH - C - CHO + CH - CH = C - CHO}\phantom{}\\
\phantom{................................................................}|\phantom{..........................}|\phantom{...........}/\phantom{.............}|\phantom{}\\
\phantom{...................................................................}\ce{CH3}\phantom{.......................}\ce{CH3}\phantom{...}\ce{H3C}\phantom{...............}\ce{CH3}\phantom{}
\end{array}\]
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संबंधित प्रश्न
Write the products formed when CH3CHO reacts with the following reagents: CH3CHO in the presence of dilute NaOH
Which of the following compounds would undergo aldol condensation, which the Cannizzaro reaction and which neither? Write the structures of the expected products of aldol condensation and Cannizzaro reaction.
- Methanal
- 2-Methylpentanal
- Benzaldehyde
- Benzophenone
- Cyclohexanone
- 1-Phenylpropanone
- Phenylacetaldehyde
- Butan-1-ol
- 2, 2-Dimethylbutanal
Write chemical equations of the following reaction :
Propanone is treated with dilute Ba (OH)2-.
Explain aldol condensation reaction in detail.
Cannizaro’s reaction is not given by ______.
Compounds A and C in the following reaction are:
\[\ce{CH3CHO ->[(i) CH3MgBr][(ii) H2O] (A) ->[H2SO4, Δ] (B) ->[Hydroboration oxidation] (C)}\]
Which of the following conversions can be carried out by Clemmensen Reduction?
(i) Benzaldehyde into benzyl alcohol
(ii) Cyclohexanone into cyclohexane
(iii) Benzoyl chloride into benzaldehyde
(iv) Benzophenone into diphenyl methane
Compound ‘A’ was prepared by oxidation of compound ‘B’ with alkaline \[\ce{KMnO4}\]. Compound ‘A’ on reduction with lithium aluminium hydride gets converted back to compound ‘B’. When compound ‘A’ is heated with compound B in the presence of \[\ce{H2SO4}\] it produces fruity smell of compound C to which family the compounds ‘A’, ‘B’ and ‘C’ belong to?
Assertion: The α-hydrogen atom in carbonyl compounds is less acidic.
Reason: The anion formed after the loss of α-hydrogen atom is resonance stabilised.
Assertion: Aromatic aldehydes and formaldehyde undergo Cannizaro reaction.
Reason: Aromatic aldehydes are almost as reactive as formaldehyde.
When liquid ‘A’ is treated with a freshly prepared ammoniacal silver nitrate solution, it gives bright silver mirror. The liquid forms a white crystalline solid on treatment with sodium hydrogensulphite. Liquid ‘B’ also forms a white crystalline solid with sodium hydrogensulphite but it does not give test with ammoniacal silver nitrate. Which of the two liquids is aldehyde? Write the chemical equations of these reactions also.
Give reasons to support the answer:
Presence of Alpha hydrogen in aldehydes and ketones is essential for aldol condensation.
Cross aldol condensation occurs between
Which of the following gives aldol con~ensation reaction?
Identify A and B from the following reaction:
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{....................}\\
\phantom{}\ce{2CH3 - C = O ->[Ba(OH)2] A ->[Δ] B + H2O}
\end{array}\]
\[\ce{CH3-CH2-CHO ->[dil][alkali] Product}\]
The product in the above reaction is:
Explain the aldol condensation of ethanal.
Which of the following does not give aldol condensation reaction?
Why is the α-hydrogens of aldehydes and ketones are acidic in nature?
Assertion (A): The final product in Aldol condensation is always α, β-unsaturated carbonyl compound.
Reason (R): α, β-unsaturated carbonyl compounds are stabilised due to conjugation.
