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प्रश्न
How will you bring about the following conversion in not more than two steps?
Ethanol to 3-Hydroxybutanal
How will you convert the following:
Ethanol to 3-Hydroxybutanal
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उत्तर १
\[\begin{array}{cc}
\phantom{...............................................................}\ce{OH}\\
\phantom{.............................................................}|\\
\ce{\underset{Ethanal}{CH3 - CH2 - OH}->[Mild oxidation][KMnO4/dil.H2SO4]\underset{(Two molecules)}{\underset{Acetaldehyde}{CH3 - CHO}}->[dil.OH-][warm]\underset{3-Hydroxybutanal}{CHO - CH2 - CH - CH3}}\
\end{array}\]
उत्तर २
\[\begin{array}{cc}
\phantom{....................................}\ce{OH}\\
\phantom{..................................}|\\
\ce{CH3CH2OH ->[PCC] CH3CHO ->[dil NaOH][Aldol condensation] \underset{3-Hydroxybutanal}{CH3 - CH - CH2 - CHO}}
\end{array}\]
PCC = Pyridinechlorochromate
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संबंधित प्रश्न
How will you convert ethanal into the following compound?
Butane-1, 3-diol
How will you bring about the following conversion in not more than two steps?
Benzaldehyde to 3-Phenylpropan-1-ol
Describe the following:
Cross aldol condensation
Complete the synthesis by giving missing starting material, reagent or product.
\[\begin{array}{cc}
\ce{C6H5CHO}\phantom{............}\\
\phantom{........}\ce{+\phantom{......}\ce{->[dil.NaOH][\Delta]}}\phantom{...}\\
\ce{CH3CH2CHO}\phantom{............}
\end{array}\]
Cannizaro’s reaction is not given by ______.
Which product is formed when the compound 
is treated with concentrated aqueous \[\ce{KOH}\] solution?
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 compounds do not undergo aldol condensation?
(i) \[\ce{CH3 - CHO}\]
(ii) 
(iii) \[\begin{array}{cc}
\phantom{}\ce{O}\\
\phantom{}||\\
\ce{CH3 - C - CH3}
\end{array}\]
(iv) \[\begin{array}{cc}
\phantom{}\ce{CH3}\\
|\phantom{...}\\
\ce{CH3 - C - CHO}\phantom{..}\\
|\phantom{...}\\
\phantom{}\ce{CH3}\\
\end{array}\]
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
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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.
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.
Which of the following does not give aldol condensation reaction?
Identify A and B:
When acetaldehyde is treated with dilute NaOH, the following reaction is observed.
\[\begin{array}{cc}
\ce{2CH3 - CHO ->[dil.NaOH] CH3 - CH - CH2 - CHO}\\
\phantom{...............}|\\
\phantom{.................}\ce{OH}
\end{array}\]
- What are the functional groups in the product?
- Can another product be formed during the same reaction? (Deduce the answer by doing atomic audit of reactant and product).
- Is this an addition reaction or condensation reaction?
