Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Class 12 Chemistry 35 Years JEE Mains &Advance Past yr Paper

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Q.1. What is the product of following reaction?    (2020)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(4)
The reaction involved is
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.2. The predominant intermolecular forces present in ethyl acetate, a liquid, are    (2020)
(1) London dispersion and dipole-dipole
(2) Hydrogen bonding and London dispersion
(3) Dipole-dipole and hydrogen bonding
(4) London dispersion, dipole-dipole and hydrogen bonding
Ans.
(1)
There are two type of forces exist in ethyl acetate a liquid. First is London dispersion forces between the hydrocarbon part of the molecule and second is dipole-dipole interaction between carbonyl carbon and oxygen of one molecule with another molecule.
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.3. The most suitable reagent for the given conversion is    (2020)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) B2H6
(2) NaBH4
(3) LiAlH4
(4) H2/Pd
Ans.
(1)
The reaction involved is
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.4. The major product in the following reaction is    (2020)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(4)
The reaction involved is
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.5. An unsaturated hydrocarbon X absorbs two hydrogen molecules on catalytic hydrogenation, and also gives following reaction
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
X will be    (2020)
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(3)
By back tracking the reaction, the aldehyde which on reaction with Tollens’ reagent gives 3-oxohexanedicarboxylic acid is
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Above product is obtained by the ozonolysis of compound given in option (3), that is,
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
The above compound can above two molecules of hydrogen to give cycloalkane.
Thus, the reaction involved is
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.6. Identify (A) in the following reaction sequence:    (2020)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(2)
Solution.
The reaction involved is
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.7. Consider the following reactions    (2020)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
The mass percentage of carbon in A is________.
Ans.
(66.67)
The reaction involved is
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
The molecular formula of A is C4H8O.
The molar mass of A = 72.0 g mL–1
Mass percentage of C Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.8. The major product of following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) RCOOH
(2) RCONH2
(3) RCHO
(4) RCH2NH2
Ans.
(3)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
The reduction of nitriles to aldehydes can be done using DIBAL-H.

Q.9. The major product formed in the following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(3)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.10. The tests performed on compound X and their inferences are:
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Compound ‘X’ is:    (2019)
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(2)
2, 4 DNP test is given by aldehydes and ketones
lodoform test is given by
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Azo dye test not given by
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.11. Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(4)
NaBH4 is a selective reducing agent, used for the reduction of aldehydes and ketones, it does not affect alkene and ester.
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.12. The major product of the following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(4)
Reaction involved:
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.13. The major product obtained in the following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans. 
(4)
Reaction involved:
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.14. The major product of the following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(4)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.15. The major product of the following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans. 
(3)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.16. The major product of the following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(3)
DIBAL-H will reduce cyanides and esters to aldehydes.
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.17. Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev cannot be prepared by:    (2019)
(1) CH3CH2COCH+ PhMgX
(2) PhCOCH2CH3 + CH3MgX
(3) PhCOCH3 + CH3CH2MgX
(4) HCHO+PhCH(CH3)CH2MgX
Ans. 
(4)
Tertiary alcohol is prepared by the reaction of Grignard reagent with a ketone (formaldehyde is used to prepare primary alcohol).
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRevPrevious year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.18. In the following reaction    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
The best combination is:
(1) CH3CHO and tBuOH
(2) HCHO and MeOH
(3) CH3CHO and MeOH
(4) HCHO and tBuOH
Ans.
(2)
Best combination is HCHO (more reactive aldehyde) and MeOH (less stericallv hindered alcohol).
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.19. In the following reactions, products A and B are:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(1)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.20. The major product of the following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans. 
(2)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
NaBH4 does not reduce the double bond but can reduce keto group Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.21. The aldehydes which will not form Grignard product with one equivalent Grignard reagents are:    (2019)
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) (B), (D)
(2) (B), (C)
(3) (B), (C), (D)
(4) (C), (D)
Ans. 
(1)
Grignard reagent will not react with aldehydes if it has a functional group which contains acidic hydrogen. Thus options (B) and (D) have—COOH and—CH2OH respectively which contain acidic H-atom. Therefore, acid-base reaction occurs.
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.22. An organic compound neither reacts with neutral ferric chloride solution nor with Fehling solution. It however, reacts with Grignard reagent and gives positive iodoform test. The compound is:    (2019)
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(4)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.23. The major product of the following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(4)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.24. The major product obtained in the following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans. 
(2)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.25. In the following reaction
Carbonyl compound + Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Rate of the reaction is the highest for:    (2019)
(1) Acetone as substrate and methanol in excess.
(2) Propanal as substrate and methanol in stoichiometric amount.
(3) Propanal as substrate and methanol in excess.
(4) Acetone as substrate and methanol in stoichiometric amount.
Ans.
(3)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Generally, aldehydes are more reactive than ketones in nucleophilic addition reactions.
∴ Rate of reaction with alcohol to form acetal and ketal is
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.26. Major products of the following reaction are:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) CH3OH and HCO2H
Ans. 
(3)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev 
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.27. Compound A(C9H10O) shows positive iodoform test. Oxidation of A with MnO4/KOH gives acid B(C8H6O4). Anhydride of B is used for the preparation of phenolphthalein. Compound A is:    (2019)
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans. 
(4)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev 

Q.28. Which dicarboxylic acid in presence of a dehydrating agent is least reactive to give an anhydride?    (2019)
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(1)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Adipic acid does not form anhydride.

Q.29. The decreasing order of ease of alkaline hydrolysis for the following esters is    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev 
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) III > II > IV > I
(2) III > II > I > IV
(3) IV > II > III > I
(4) II > III > I > IV
Ans.
(2)
Rate of reaction ∝ Electrophilicity of carbonyl carbon, so, E.W.G. increases rate while E.R.G. decreases the rate.
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.30. The major product of the following reaction is:    (2019)
CH3CH = CHCO2CH3 Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) CH3CH2CH2CO2CH3
(2) CH3CH = CHCH2OH
(3) CH3CH2CH2CH2OH
(4) CH3CH2CH2CHO
Ans.
(2)
LiAlH4 reduces esters to alcohols but does not reduce C = C.
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.31. The major product of the following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(1)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Acid catalysed intramolecular esterification reaction.
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.32. The major product of the following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3)Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(2)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.33. The major product ‘Y’ in the following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans. 
(1)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.34. The major product of the following reaction is:    (2019)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(2)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev 

Q.35. The main reduction product of the following compound with NaBH4 in methanol is:    (2018)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(1)
Sodium borohydride will reduce ketone to alcohol. It will not reduce amide group and C = C double bond.
Hence, option (1) is the correct answer.

Q.36. The reagent(s) required for the following conversion are:    (2018)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) (i)LiAlH4 (ii) H3 O+ 
(2) (i) B2 H6 (ii) SnCl2/HCl  (iii) H3O+ 
(3) (i)B2H6  (ii)DIBAL-H (iii)H3O+ 
(4) (i)NaBH4 (ii)Raney Ni/H2 (iii)H3O+ 
Ans.
(3)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.37. The major product B formed in the following reaction sequence is:   (2018)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(4)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRevPrevious year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.38. The correct sequence of reagents for the following conversion will be    (2017)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) [Ag(NH3)2]+OH-, H+/CH3OH, CH3MgBr 
(2) CH3MgBr, H+/CH3OH, [Ag(NH3)2]+OH- 
(3) CH3MgBr, [Ag(NH3)2]+OH-, H+/CH3OH 
(4) [Ag(NH3)2]+OH-, CH3MgBr, H+/CH3OH 
Ans.
(1)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.39. The major product obtained in the following reaction is    (2017)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans. (2) 
DIBAL — H reduces esters and carboxylic acids into aldehydes 
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.40. A compound of molecular formula C8H8O2 reacts with acetophenone to form a single cross-aldol product in the presence of base. The same compound on reaction with conc. NaOH forms bezyl alcohol as one of the products. The structure of the compound is:    (2017)
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(1)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev 
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.41. The reaction of propene with HOCl (Cl2 + H2O) proceeds through the intermediate:    (2016) 
(1) CH3 - CH+ - CH2 - OH 
(2) CH3 - CH+ - CH2 - Cl 
(3) CH3 - CH(OH) - CH+2 
(4) CH3 - CHCl - CH+2 
Ans.
(2)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.42. The correct statement about the synthesis of erythritol (C(CH2OH)4) used in the preparation of PETN is:    (2016)
(1) The synthesis requires two aldol condensations and two Cannizzaro reactions.
(2) Alpha hydrogens of ethanol and methanol are involved in this reaction.
(3) The synthesis requires four aldol condensations between methanol and ethanol.
(4) The synthesis requires three aldol condensations and one Cannizzaro reaction.
Ans.
(4)
The synthesis requires three aldol & one cannizzaro reaction.
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev

Q.43. Consider the reaction sequence below:    (2016)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(1) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(2) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(3) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
(4) Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev
Ans.
(4)
Previous year Questions (2016-20) - Aldehydes, Ketones and Carboxylic Acids Notes | EduRev 

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