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प्रश्न
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.
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उत्तर
The possible products of aldol condensation from propanal and butanal are:
(i) \[\begin{array}{cc}
\phantom{..............................}\ce{OH}\phantom{...}\ce{CH3}\\
\phantom{...........................}|\phantom{.....}|\\
\ce{\underset{Propanal}{2CH3CH2CHO}->[dil.\overset{-}{O}H]\underset{3-Hydroxy-2-methylpentanal}{H3C - CH2 - CH - CH - CHO}}\\
\end{array}\]
(ii) \[\begin{array}{cc}
\phantom{.......................................}\ce{OH}\phantom{..}\ce{CH2CH3}\\
\phantom{................................}|\phantom{.....}|\\
\ce{\underset{Butanal}{2CH3(CH2)2CHO}->[dil.\overset{-}{O}H]\underset{2-Ethyl-3-hydroxyhexanal}{H3C - (CH2)2 - CH - CH - CHO}}\
\end{array}\]
(iii) When butanal acts as an electrophile and propanal as a nucleophile:
\[\begin{array}{cc}
\phantom{...........................................}\ce{OH}\\
\phantom{.........................................}|\\
\ce{\underset{Butanal}{H3C - (CH2)2CHO} + \underset{Propanal}{CH3CH2CHO}->[\overset{-}{O}H]H3C - (CH2)2 - CH - CH - CHO}\\
\phantom{.....................................................}|\\
\phantom{.........................................................}\ce{\underset{3-Hydroxy-2-methylhexanal}{CH3}}\
\end{array}\]
(iv) When propanal serves as an electrophile and butanal as a nucleophile:
\[\begin{array}{cc}
\phantom{............................................}\ce{OH}\phantom{...}\ce{C2H5}\\
\phantom{.........................................}|\phantom{......}|\\
\ce{CH3CH2CHO + CH3(CH2)2CHO -> \underset{2-Ethyl-3-hydroxypentanal}{H3C - CH2 - CH - CH - CHO}}\
\end{array}\]
APPEARS IN
संबंधित प्रश्न
Write the products formed when CH3CHO reacts with the following reagents: CH3CHO in the presence of dilute NaOH
Describe the following:
Cross aldol condensation
Complete the synthesis by giving missing starting material, reagent or product.
\[\begin{array}{cc}
\ce{C6H5CHO}\phantom{............}\\
\phantom{........}\ce{+\phantom{......}\ce{->[dil.NaOH][\Delta]}}\phantom{...}\\
\ce{CH3CH2CHO}\phantom{............}
\end{array}\]
Why is alpha (α) hydrogen of carbonyl compounds acidic in nature?
Write chemical equations of the following reaction :
Propanone is treated with dilute Ba (OH)2-.
Write chemical equations of the following reaction :
Benzoyl chloride is hydrogenated in the presence of `"Pd"/(BaSO_4)`
Write a chemical equation for the following reaction:
Propanone is treated with dilute Ba( OH)2.
Which product is formed when the compound
is treated with concentrated aqueous \[\ce{KOH}\] solution?
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) \[\begin{array}{cc}
\phantom{}\ce{CH3}\\
|\phantom{...}\\
\ce{CH3 - C - CHO}\phantom{..}\\
|\phantom{...}\\
\phantom{}\ce{CH3}\\
\end{array}\]
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.
Convert the following:
Acetaldehyde to But-2-enal
\[\ce{CH3-CH2-CHO ->[dil][alkali] Product}\]
The product in the above reaction is:
Explain Aldol condensation of ethanal.
Which of the following compounds will undergo self-condensation in the presence of dilute NaOH solution?
Why is the α-hydrogens of aldehydes and ketones are acidic in nature?

Identify A and B:
Write a note on the aldol condensation reaction of acetaldehyde.
What is aldol condensation? Explain it with suitable examples.
