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How will you convert ethanal into the following compound? Butane-1, 3-diol - Chemistry

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प्रश्न

How will you convert ethanal into the following compound?

Butane-1, 3-diol

रासायनिक समीकरण/संरचनाएँ

उत्तर

\[\ce{\underset{Ethanal}{2CH3CHO}->[Dil.NaOH][Aldol condensation]\underset{3-Hydroxybutanal}{\overset{4}{C}H3\overset{3}{C}HOH - \overset{2}{C}H2 - \overset{1}{C}HO}->[NaBH4][(Reduction)]\underset{Butane-1, 3-diol}{\overset{4}{C}H3 - \overset{3}{C}HOH - \overset{2}{C}H2 - \overset{1}{C}H2OH}}\]

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अध्याय 12: Aldehydes, Ketones and Carboxylic Acids - Exercises [पृष्ठ ३७८]

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एनसीईआरटी Chemistry [English] Class 12
अध्याय 12 Aldehydes, Ketones and Carboxylic Acids
Exercises | Q 8.1 | पृष्ठ ३७८

संबंधित प्रश्न

Write the products formed when CH3CHO reacts with the following reagents: CH3CHO in the presence of dilute NaOH


What is meant by the following term? Give an example of the reaction in the following case.

Aldol


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.

  1. Methanal
  2. 2-Methylpentanal
  3. Benzaldehyde
  4. Benzophenone
  5. Cyclohexanone
  6. 1-Phenylpropanone
  7. Phenylacetaldehyde
  8. Butan-1-ol
  9. 2, 2-Dimethylbutanal

How will you bring about the following conversion in not more than two steps?

Ethanol to 3-Hydroxybutanal


Write chemical equations of the following reaction : 

Propanone is treated with dilute Ba (OH)2-.


Write a chemical equation for the following reaction: 
Propanone is treated with dilute Ba( OH)2.


What is substituted imine called?


Compounds A and C in the following reaction are:

\[\ce{CH3CHO ->[(i) CH3MgBr][(ii) H2O] (A) ->[H2SO4, Δ] (B) ->[Hydroboration oxidation] (C)}\]


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.


Give reasons to support the answer:

Presence of Alpha hydrogen in aldehydes and ketones is essential for aldol condensation.


\[\ce{CH3-CH2-CHO ->[dil][alkali] Product}\]

The product in the above reaction is:


Explain 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.


Write a note on the aldol condensation reaction of acetaldehyde.


What is aldol condensation? Explain it with suitable examples.


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