Q45.Arrange the following compounds in order of decreasing acidity : (1) III > I > II > IV (2) IV > III > I > II (3) II > IV > I > III (4) I > II > III > IV
What This Question Tests
This question evaluates the ability to compare and arrange different organic compounds in order of their decreasing acidity, considering the electronic effects influencing conjugate base stability.
Concepts Tested
π NCERT Sections This Tests
7.8 β Ortho And Para Nitrophenols Are More Acidic Than Phenol. Draw The
Chemistry Class 12 Β· Chapter 7
7.8 Ortho and para nitrophenols are more acidic than phenol. Draw the resonance structures of the corresponding phenoxide ions.
7.14 β Give Two Reactions That Show The Acidic Nature Of Phenol. Compare Acidity
Chemistry Class 12 Β· Chapter 7
7.14 Give two reactions that show the acidic nature of phenol. Compare acidity of phenol with that of ethanol.
7.7 β Predict The Major Product Of Acid Catalysed Dehydration Of
Chemistry Class 12 Β· Chapter 7
7.7 Predict the major product of acid catalysed dehydration of (i) 1-methylcyclohexanol and (ii) butan-1-ol
π Question Details
- Chapter
- Alcohols Phenols Ethers
- Topic
- Acidity of organic compounds
- Year
- 2013
- Shift
- 07 Apr
- Q Number
- Q45
- Type
- MCQ
- NCERT Ref
- Class 12 Chemistry Ch 11: Alcohols Phenols Ethers
More from this Chapter
Q68.Phenol, when it first reacts with concentrated sulphuric acid and then with concentrated nitric acid, gives (1) 2,4,6-trinitrobenzene (2) o-nitrophenol (3) p-nitrophenol (4) nitrobenzene
Q41.The number of stereoisomers possible for a compound of the molecular formula CH3 βCH = CH βCH(OH) βMe is : (1) 3 (2) 2 (3) 4 (4) 6
Q56.The major product obtained on interaction of phenol with sodium hydroxide and carbon dioxide is : (1) benzoic acid (2) salicylaldehyde (3) salicylic acid (4) phthalic acid
Q43.The edge length of a face centered cubic cell of an ionic substance is 508pm. If the radius of the cation is 110pm, the radius of the anion is (1) 288pm (2) 398pm (3) 618pm (4) 144pm