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प्रश्न
\[\ce{CH3Br ->[KNC] (A) ->[H3O^+] (B) ->[PCl5] (C)}\] product (C) is:
पर्याय
acetyl chloride
chloro acetic acid
α-chlorocyano ethanoic acid
none of these
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उत्तर
acetyl chloride
APPEARS IN
संबंधित प्रश्न
Answer in brief.
Write reaction showing conversion of Acetaldehyde into acetaldehyde dimethyl acetal.
Acetone reacts with iodine (I2) to form iodoform, in the presence of ____________.
\[\begin{array}{cc} \phantom{...}\ce{R}\phantom{.................}\ce{R}\phantom{..}\ce{H}\phantom{................}\\ \phantom{...}\backslash\phantom{..................}\backslash/\phantom{..........}\phantom{.......}\\ \ce{C = O ->[H2NNH2][KOH/glycol] C + N2 + H2O}\\ \phantom{}/\phantom{............}\phantom{.......}/\phantom{}\backslash\phantom{...............}\\ \phantom{}\ce{R}\phantom{..................}\ce{R}\phantom{..}\ce{H}\phantom{...............} \end{array}\]
Reaction is called ____________.
Which of the following carbonyl compounds does NOT undergo aldol condensation?
Identify the product Y in the following series of reactions.
\[\ce{4-Nitrotoluene ->[(CH3CO)2O/CrO3][273 - 278 K] X ->[H3O^+][\Delta] Y}\]
Write the structure of the major product of the aldol condensation of benzaldehyde with acetone.
How will you prepare cinnamic acid from benzaldehyde?
Which of the following compounds is most reactive towards nucleophilic addition reactions?
Aldehydes are readily oxidised to yield carboxylic acids but ketones are inert to oxidation. Which is the most likely explanation regarding this difference in reactivity?
Write the structure of the major product of the aldol condensation of benzaldehyde with acetone.
