Which of the following represents the correct order of acidity in the given compounds?

1. FCH2COOH > CH3COOH > BrCH2COOH > ClCH2COOH

2. BrCH2COOH > ClCH2COOH > FCH2COOH > CH3COOH

3. FCH2COOH > ClCH2COOH > BrCH2COOH > CH3COOH

4. CH3COOH > BrCH2COOH > ClCH2COOH > FCH2COOH 

Subtopic:  Acidic & Basic Character |
 86%
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Among the following, the strongest acid is:

1. CH3COOH 2. CH2ClCH2COOH
3. CH2ClCOOH 4. CH3CH2COOH
Subtopic:  Acidic & Basic Character |
 77%
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The distance between two adjacent carbon atoms is largest in

1. Benzene             

2. Ethene

3. Butane              

4. Ethyne

Subtopic:  Hybridisation & Structure of Carbon Compounds |
 86%
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Which of the following represent the correct decreasing order of acidic strength of following? 

(i) Methanoic acid

(ii) Ethanoic acid

(iii) Propanoic acid

(iv) Butanoic acid

1. (i)>(ii)>(iii)>(iv)

2. (ii)>(iii)>(iv)>(i)

3. (i)>(iv)>(iii)>(ii)

4. (iv)>(i)>(iii)>(ii)

Subtopic:  Acidic & Basic Character |
 88%
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The IUPAC name of the compound,

 is-

1. 1, 3-Dibromo-3-methylbutane

2. 3-Methyl-1,2-bromobutane

3. 3-Methyl-1,3-bromopropane

4. None of the above

Subtopic:  Nomenclature |
 79%
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Which one of the following has the shortest carbon-carbon bond length?                      

1. Benzene                     

2. Ethene

3. Ethyne                         

4. Ethane

Subtopic:  Hybridisation & Structure of Carbon Compounds |
 86%
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The shortest C-C bond distance is found in               

1. Diamond             

2. Ethane

3. Benzene             

4. Acetylene

Subtopic:  Hybridisation & Structure of Carbon Compounds |
 66%
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What is decreasing order of basicity of 1°, 2° and 3° ethyl amines and ammonia in aqueous medium?          

1. NH3>C2H5NH2>(C2H5)2NH>(C2H5)3N

2. (C2H5)3N>(C2H5)2NH>C2H5NH2> NH3

3. (C2H5)3NH>C2H5NH2>(C2H5)3N>NH3

4. (C2H5)2NH>(C2H5)3N>C2H5NH2>NH3

Subtopic:  Acidic & Basic Character |
 58%
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The cylindrical shape of an alkyne is due to the presence of- 

1. Three sigma C-C bonds

2. Three π C-C bonds

3. Two sigma C-C and one π C-C bonds

4. One sigma C-C and two π C-C bonds

Subtopic:  Hybridisation & Structure of Carbon Compounds |
 80%
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The (R)- and (S)-enantiomers of an optically active compound differ in

1. their solubility in a chiral solvent

2. their reactivity with a chiral reagent

3. their optical rotation of plane polarised light

4. their melting points

Subtopic:  Stereo Isomers |
 90%
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