Advertisements
Advertisements
Question
\[\ce{Ethanoic acid ->[P/Br2] 2-bromoethanoic acid}\]. This reaction is called ____________.
Options
Finkelstein reaction
Haloform reaction
Hell-Volhard-Zelinsky reaction
None of these
Advertisements
Solution
\[\ce{Ethanoic acid ->[P/Br2] 2-bromoethanoic acid}\]. This reaction is called Hell-Volhard-Zelinsky reaction.
APPEARS IN
RELATED QUESTIONS
Identify B in the following reaction,
\[\ce{Acetaldoxime ->[Na][alcohol] A ->[NaNO2][HCl] B + H2O + N2\uparrow}\]
Compounds of general formula, are called ____________.
\[\begin{array}{cc} \phantom{...}\ce{R}\phantom{....}\ce{OR''}\phantom{}\\ \phantom{}\backslash\phantom{..}/\\ \ce{C}\\ \phantom{}/\phantom{..}\backslash\\ \phantom{...}\ce{R'}\phantom{...}\ce{OR''}\phantom{} \end{array}\]
Predict the product Z in the following series of reactions.
\[\ce{Ethanoic acid ->[PCl5] X ->[C6H6][Anhydrous AlCl3] Y ->[i) CH3MgBr][H3O^+] Z}\]
Phenyl methanal is reacted with concentrated NaOH to give two products X and Y. X reacts with metallic sodium to liberate hydrogen X and Y are ____________.
Identify A, B, C and D.
\[\ce{ethanoic acid ->[SOCl2] A ->[Pd/BaSO4] B ->[NaOH] C ->[][\Delta] D}\]
What is the action of HCN on 2, 4-dichlorobenzaldehyde?
How propanal is converted into propane.
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?
How will you prepare Acetic anhydride from acetic acid.
Write the structure of the major product of the aldol condensation of benzaldehyde with acetone.
