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complete the following reaction:

Concept: Aldehydes and Ketones >> Chemical Reactions of Aldehydes and Ketones - Other Reactions
complete the following reaction:
\[\begin{array}{cc}
\phantom{...}\ce{CH3} \\
| \\
\phantom{.................}\ce{CH3-CH-COOH ->[(i) Br2/Red P4][(ii)H2O]}
\end{array}\]
Concept: Aldehydes and Ketones >> Chemical Reactions of Aldehydes and Ketones - Other Reactions
Write a chemical reaction to show that the open structure of D-glucose contains the following :
Aldehyde as a carbonyl group
Concept: Aldehydes and Ketones >> Structure of the Carbonyl Group
Give a reason for the following :
N-N bond is weaker than the P-P bond.
Concept: Acids >> Chemical Reactions of Carboxylic Acids - Reactions Involving –COOH Group
Complete the following reaction:

Concept: Aldehydes and Ketones >> Chemical Reactions of Aldehydes and Ketones - Other Reactions
Complete the following reaction:
\[\ce{(C6H5CH2)2Cd + 2CH3COCI}\]
Concept: Preparation of Aldehydes and Ketones
An alkene ‘A’ (Mol. formula \[\ce{C5H10}\]) on ozonolysis gives a mixture of two compounds ‘B’ and ‘C’. Compound ‘B’ gives positive Fehling’s test and also forms iodoform on treatment with \[\ce{I2}\] and \[\ce{NaOH}\]. Compound ‘C’ does not give Fehling’s test but forms iodoform. Identify the compounds A, B and C. Write the reaction for ozonolysis and formation of iodoform from B and C.
Concept: Aldehydes and Ketones >> Preparation of Aldehydes
Arrange the following in the increasing order of their property indicated:
Acetaldehyde, Acetone, Methyl tert butyl ketone (reactivity towards NH2OH).
Concept: Aldehydes and Ketones >> Nomenclature of Aldehydes and Ketones
Give reasons to support the answer:
Presence of Alpha hydrogen in aldehydes and ketones is essential for aldol condensation.
Concept: Aldehydes and Ketones >> Chemical Reactions of Aldehydes and Ketones - Reactions Due to α-hydrogen
Write the IUPAC name for the following organic compound:

Concept: Aldehydes and Ketones >> Nomenclature of Aldehydes and Ketones
Complete the following:
\[\ce{C6H5NO2 ->[Sn/HCl] A ->[Br2/H2O] B ->[NaNO2/HCl][273 - 278 K] C ->[HBF4][Δ] D}\]
Concept: Acids >> Nomenclature of Carboxylic Acids
Which of the following tests/reactions is given by aldehydes as well as ketones?
Concept: Aldehydes and Ketones >> Chemical Reactions of Aldehydes and Ketones - Oxidation
The oxidation of toluene to benzaldehyde by chromyl chloride is called ______.
Concept: Aldehydes and Ketones >> Preparation of Aldehydes
Write the reaction and IUPAC name of the product formed when 2-Methylpropanal (isobutyraldehyde) is treated with ethyl magnesium bromide followed by hydrolysis.
Concept: Aldehydes and Ketones >> Nomenclature of Aldehydes and Ketones
Write the equations for the following reaction:
Salicylic acid is treated with acetic anhydride in the presence of conc H2SO4
Concept: Acids >> Chemical Reactions of Carboxylic Acids - Reactions Involving Cleavege of C-OH Bond
A hydrocarbon (A) with molecular formula C5H10 on ozonolysis gives two products (B) and (C). Both (B) and (C) give a yellow precipitate when heated with iodine in presence of NaOH while only (B) give a silver mirror on reaction with Tollen’s reagent.
- Identify (A), (B) and (C).
- Write the reaction of B with Tollen’s reagent.
- Write the equation for iodoform test for C.
- Write down the equation for aldol condensation reaction of B and C.
Concept: Aldehydes and Ketones >> Chemical Reactions of Aldehydes and Ketones - Oxidation
Arrange the following in the increasing order of their property indicated:
Ethanal, Propanone, Propanal, Butanone (reactivity towards nucleophilic addition)
Concept: Aldehydes and Ketones >> Chemical Reactions of Aldehydes and Ketones - Nucleophilic Addition Reactions
Write the IUPAC name of the following complex:
K2[PdCl4]
Concept: Aldehydes and Ketones >> Nomenclature of Aldehydes and Ketones
Explain the following reactions:
Clemmensen reaction
Concept: Aldehydes and Ketones >> Chemical Reactions of Aldehydes and Ketones - Reduction
Explain the following reactions:
Stephan reaction
Concept: Aldehydes and Ketones >> Preparation of Aldehydes
