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प्रश्न
Explain haloform reaction with suitable example.
Write a note on the Haloform reaction.
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उत्तर
- This reaction is given by acetaldehyde, all methyl ketones (CH3–CO–R), and all alcohols containing CH3(CHOH)– group.
- When an alcohol or methyl ketone is warmed with sodium hydroxide and iodine, a yellow precipitate is formed. Here the reagent sodium hypoiodite is produced in situ.
- During the reaction, the sodium salt of the carboxylic acid is formed which contains one carbon atom less than the substrate.
- The methyl group is converted into haloform (CHX3).
e.g. Acetone is oxidized by sodium hypoiodite to give sodium salt of acetic acid and yellow precipitate of iodoform.
\[\begin{array}{cc}
\phantom{..}\ce{O}\phantom{.......................................}\ce{O}\phantom{..........................}\\
\phantom{..}||\phantom{.......................................}||\phantom{..........................}\\
\ce{\underset{\text{Acetone}}{CH3 - C - CH3} + \underset{\text{Sodium hypoiodite}}{3NaOI} ->[NaOH/I2][\Delta] \underset{\text{Sodium acetate}}{CH3 - C - O- Na+} + \underset{\text{Iodoform}}{CHI3 ↓} + 2NaOH}
\end{array}\]
संबंधित प्रश्न
Write a note on Stephen reaction.
Answer in brief.
Write reaction showing conversion of Acetaldehyde into acetaldehyde dimethyl acetal.
_____________ reaction is used to synthesize straight alkyl substituted benzenes.
Write the name of the product when ketones react with 1,2-diol in presence of dry HCl.
Identify the INCORRECT reaction.
Identify B in the following reaction,
\[\ce{Acetaldoxime ->[Na][alcohol] A ->[NaNO2][HCl] B + H2O + N2\uparrow}\]
If acetaldehyde is treated with Fehling's solution, the change that occurs in the system is ____________.
Which of following is not a property of red phosphorus?
Compounds of general formula, are called ____________.
\[\begin{array}{cc} \phantom{...}\ce{R}\phantom{....}\ce{OR''}\phantom{}\\ \phantom{}\backslash\phantom{..}/\\ \ce{C}\\ \phantom{}/\phantom{..}\backslash\\ \phantom{...}\ce{R'}\phantom{...}\ce{OR''}\phantom{} \end{array}\]
\[\begin{array}{cc} \phantom{...}\ce{R}\phantom{.................}\ce{R}\phantom{..}\ce{H}\phantom{................}\\ \phantom{...}\backslash\phantom{..................}\backslash/\phantom{..........}\phantom{.......}\\ \ce{C = O ->[H2NNH2][KOH/glycol] C + N2 + H2O}\\ \phantom{}/\phantom{............}\phantom{.......}/\phantom{}\backslash\phantom{...............}\\ \phantom{}\ce{R}\phantom{..................}\ce{R}\phantom{..}\ce{H}\phantom{...............} \end{array}\]
Reaction is called ____________.
An aldehyde or ketone reacts with hydrogen cyanide to form corresponding cyanohydrin derivatives. This reaction is an example of ____________.
Which of the following does not give yellow solid on treatment with sodium hypoiodlte?
Which of the following will give positive iodoform test?
Following reaction is an example of ____________.
\[\ce{Benzaldehyde ->[Nitration] {m}-Nitrobenzaldehyde}\]
Which of the following is a Wolf - Kishner reduction?
\[\ce{Ethanoic acid ->[P/Br2] 2-bromoethanoic acid}\]. This reaction is called ____________.
\[\ce{CH3Br ->[KNC] (A) ->[H3O^+] (B) ->[PCl5] (C)}\] product (C) is:

‘B’ is:
In which case, chiral carbon is not generated by reaction with HCN.
Write the structure of the major product of the aldol condensation of benzaldehyde with acetone.
Identify A, B and C.

How will you prepare acetic anhydride from acetic acid?
How will you prepare ethane from sodium acetate?
How will you prepare acetaldehyde from ethyne?
Which of the following compound will show a positive silver mirror test?
Which of the following is not correctly matched?
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?
Give two examples which undergo Wolf-Kishner reduction.
Write a note on Clemmensen reduction.
What is the action of the following regent on propanal?
Sodium Bisulphite
