JEE Questions for Chemistry Aldehydes Ketones And Carboxylic Acids Quiz 15 - MCQExams.com

Which of the following orders of relative strengths of acids is correct ?
  • FCH2COOH > ClCH2COOH > BrCH2COOH
  • ClCH2COOH > BrCH2COOH > FCH2COOH
  • BrCH2COOH > ClCH2COOH > FCH2COOH
  • ClCH2CO2H > FCH2COOH > BrCH2COOH
Lactic acid on oxidation by alkaline potassium permanganate gives
  • tartaric acid
  • pyruvic acid
  • cinnamic acid
  • propionic acid
The reaction,
Chemistry-Aldehydes Ketones and Carboxylic Acids-809.png
  • Reimer –Tiemann reaction
  • Hell-Volhard Zelinsky reaction
  • Cannizzaro reaction
  • Sandmeyer reaction

Chemistry-Aldehydes Ketones and Carboxylic Acids-810.png
  • Wurtz reaction
  • Koch reaction
  • Clemmensen reduction
  • Kolbe’s reaction
Which of the following acids has the smallest dissociation constant ?
  • CH3CHFCOOH
  • FCH2CH2COOH
  • BrCH2CH2COOH
  • CH3CHBrCOOH
Identify the correct order of boiling points of the following compounds :
1. CH3CH2CH3CH3OH
2. CH3CH2CH2CHO
3.CH3CH2CH2COOH
  • 1 > 2 > 3
  • 3 >1 >2
  • 1 > 3 > 2
  • 3 > 2 > 1

Chemistry-Aldehydes Ketones and Carboxylic Acids-811.png
  • CH3CH2COCl
  • CH3CH2CHO
  • CH2 = CHCOOH
  • ClCH2CH2COOH
In the following sequence of reactions, what is D ?
Chemistry-Aldehydes Ketones and Carboxylic Acids-813.png
  • primary amine
  • an amide
  • phenyl isocyanate
  • a chain lengthened hydrocarbon
The general formula CnH2nO2 could be for open chain
  • Dialdehyde
  • Diketones
  • Carboxylic acids
  • Diols
In the set of the given reactions, acetic acid yielded a product C.
Chemistry-Aldehydes Ketones and Carboxylic Acids-815.png
  • CH3CH(OH)C2H5
  • CH3COC6H5

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-816.png
  • CH3CH(OH) C6H5
Which one of the following orders of acid strength is correct?
  • RCOOH > ROH >HOH > HC ≡ CH
  • RCOOH >HOH >ROH> HC ≡ CH
  • RCOOH > HC CH > HO ≡ H >ROH
  • RCOOH > HC ≡ CH > HOH > ROH
End product of the following sequence of reactions is

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-818.png
  • 2)
    Chemistry-Aldehydes Ketones and Carboxylic Acids-819.png
  • CH2(COOH)2

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-820.png
Consider the following reaction sequence:
Chemistry-Aldehydes Ketones and Carboxylic Acids-822.png
  • CH3 — CH(COOH)2, CH3CH2COOH
  • 2)
    Chemistry-Aldehydes Ketones and Carboxylic Acids-823.png

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-824.png

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-825.png
Consider the following reaction
Chemistry-Aldehydes Ketones and Carboxylic Acids-826.png
  • CH3COOC2H5, (CH3)3 COH
  • HCOOC2H7, (CH3)2CHOH
  • C2H5COOCH3, (C2H5)3COH
  • HCOOC3H7, (CH3)3COH
A keto ester (A) with M.F. C6H10O3 on treatment with NaOH + I2 does not give iodoform but on boiling with dilute KOH gives a compound (B) with M.F. C4H5O3K which upon acidification followed by heating undergoes decarboxylation to give acetone. The keto ester (A) is
  • CH3COCH2CH2COOCH3
  • CH3COCH2COOC2H5
  • CH3CH2OCH2COOCH3
  • CH3 - COCH(CH3)COOCH3

Chemistry-Aldehydes Ketones and Carboxylic Acids-829.png
  • Picric acid ,2, 4, 6-Tribromophenol
  • 5-Nitrosalicylic acid, 5-bromosalicylic acid
  • o-Nitrophenol, o-bromophenol
  • 3,5-Dinitrosalicylic acid, 3,5-dibromo-salicylic acid
The pKa value of the C-H acids MeC ≡ CH(I). MeCOCH2COOEt (II), MeCOOEt (III) and PhMe (IV) decreases as
  • I > III > IV > II
  • II > IV > III >I
  • IV > III > I > II
  • I > IV > III > II
Consider the reaction,
Chemistry-Aldehydes Ketones and Carboxylic Acids-832.png

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-833.png
  • 2)
    Chemistry-Aldehydes Ketones and Carboxylic Acids-834.png

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-835.png
  • Both (and (2)
The major product expected from monobromination of phenyl benzoate is

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-837.png
  • 2)
    Chemistry-Aldehydes Ketones and Carboxylic Acids-838.png

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-839.png

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-840.png

Chemistry-Aldehydes Ketones and Carboxylic Acids-842.png

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-843.png
  • 2)
    Chemistry-Aldehydes Ketones and Carboxylic Acids-844.png

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-845.png

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-846.png
The product (A) of the following reaction,
Chemistry-Aldehydes Ketones and Carboxylic Acids-848.png

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-849.png
  • 2)
    Chemistry-Aldehydes Ketones and Carboxylic Acids-850.png

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-851.png

  • Chemistry-Aldehydes Ketones and Carboxylic Acids-852.png
Ease of esterification of the following alcohols CH3CH2OH (I), (CH3)2CHOH (II) (CH3)3COH (III) with HCOOH is
  • I < II < III
  • III < II < I
  • II < I < III
  • I = II = III
The ease of esterification of the following acids HCOOH (I), CH3COOH (II), CH3CH2COOH (III) with CH3OH is
  • III < II < I
  • I < II < III
  • II < I < III
  • I = II = III
In the following reaction,
Chemistry-Aldehydes Ketones and Carboxylic Acids-854.png
  • NH3 and CH3CONH2
  • NH3 and CH3NH2
  • HN3 and CH3CONH2
  • HN3 and CH3NH2
Which of the following will evolve N2 gas when treated with Br2 / KOH?
  • NH2CONH2
  • CH3CONH2
  • HCONH2
  • C6H5CONHCH3
Consider the following reaction :
Chemistry-Aldehydes Ketones and Carboxylic Acids-857.png
  • Hell-Volhard Zelinsky, carbanion
  • Sandmeyer, free radical
  • Wolff, carbene
  • Hunsdiecker, free radical

Chemistry-Aldehydes Ketones and Carboxylic Acids-858.png
  • Acrylic acid
  • Glycine
  • Anthranilic acid
  • Chloroacetic acid

Chemistry-Aldehydes Ketones and Carboxylic Acids-860.png
  • Phthalic acid, o-benzoylbenzoic acid
  • o-Benzoylbenzoic acid ,anthraquinone
  • Anthracene, phthalic acid
  • Anthrone, anthraquinone
The products A, B and C in the following sequence of reactions respectively are
Chemistry-Aldehydes Ketones and Carboxylic Acids-862.png
  • Cyclohexanone, benzoic acid, benzyl alcohol
  • Cyclohexanone, benzaldehyde, 2-benzylidenecyclohexanone
  • Cyclohexanecarboxaldehyde, benzaldehyde, benzyl alcohol
  • Cyclohexanone, benzaldehyde, 2-bezylethenecyclohexanone
Different possible thermal decomposition pathways for peroxyesters are shown below. Match each pathway from Column I and select the correct answer using the code given below the lists.
Chemistry-Aldehydes Ketones and Carboxylic Acids-864.png
  • P = 1, Q = 3, R = 4, S = 2
  • P = 2, Q = 4, R = 3, S = 1
  • P = 4, Q = 1, R = 2, S = 3
  • P = 3, Q = 2, R = 1, S = 4
0:0:1


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