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प्रश्न
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?
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उत्तर
When alkaline \[\ce{KMnO4}\] oxidises compound ‘B’ with compound ‘A’, acid is formed.
\[\ce{B ->[{[O]}][alkaline KMnO4] A -> acid}\]
When compound ‘A’ is reduced with \[\ce{LiAlH4}\], it transforms into compound ‘B’. The letter ‘B’ stands for a type of alcoholic beverage.
\[\ce{A ->[LiAlH4] B -> Alcohol}\]
When compounds ‘A’ and ‘B’ are heated with conc. \[\ce{H2SO4}\], compound ‘C’ is formed which has a fruity odour.
\[\ce{A + B ->[A][H2SO4] fruitysmell (ester)}\]
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संबंधित प्रश्न
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.
- Methanal
- 2-Methylpentanal
- Benzaldehyde
- Benzophenone
- Cyclohexanone
- 1-Phenylpropanone
- Phenylacetaldehyde
- Butan-1-ol
- 2, 2-Dimethylbutanal
Write structural formulas and names of four possible aldol condensation products from propanal and butanal. In each case, indicate which aldehyde acts as nucleophile and which as electrophile.
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.
\[\begin{array}{cc}
\ce{C6H5CHO}\phantom{............}\\
\phantom{........}\ce{+\phantom{......}\ce{->[dil.NaOH][\Delta]}}\phantom{...}\\
\ce{CH3CH2CHO}\phantom{............}
\end{array}\]
Give reasons Acetylation of aniline reduces its activation effect.
Why is alpha (α) hydrogen of carbonyl compounds acidic in nature?
Write a chemical equation for the following reaction:
Propanone is treated with dilute Ba( OH)2.
What is substituted imine called?
Explain aldol condensation reaction in detail.
Which product is formed when the compound 
is treated with concentrated aqueous \[\ce{KOH}\] solution?
Compounds A and C in the following reaction are:
\[\ce{CH3CHO ->[(i) CH3MgBr][(ii) H2O] (A) ->[H2SO4, Δ] (B) ->[Hydroboration oxidation] (C)}\]
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.
Why are carboxylic acids more acidic than alcohols or phenols although all of them have hydrogen atom attached to a oxygen atom \[\ce{(-O-H)}\]?
Convert the following:
Acetaldehyde to But-2-enal
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?
Write a note on the aldol condensation reaction of acetaldehyde.
