The solubility of phenol in water is lower. This can be attributed to:

1. Non-polar nature of phenol

2. Acidic nature of -OH group

3. Non-polar hydrocarbon part in phenol

4. None of the above

Phenol and benzoic acid can be distinguished by:

1. Aqueous NaHCO₃                           

2. Aqueous NaNO₃

3. Aqueous NaOH                               

4. Conc. H₂SO₄

The products formed in the following reaction, C₆H₅-O-CH₃ + HI $\stackrel{\mathrm{Heat}}{\to }$ are-

1. C₆H₅OH and CH₃I 

2. C₆H₅I and CH₃OH

3. C₆H₅CH₃ and HOI

4. C₆H₆ and CH₃OI

The order of decreasing acidic character of cyclohexanol (I),
acetic acid (II),
2,4,6-trinitrophenol (III),
and phenol (IV), is -                                                     

1. III>II>IV>I 

2. II>III>I>IV

3. II>III>IV>I 

4.  III>IV>II>I

Consider the following reaction,

Phenol$\stackrel{\mathrm{Zn}-\mathrm{dust}}{\to }$X$\underset{\mathrm{Anhy}.{\mathrm{AlCl}}_3}{\overset{{\mathrm{CH}}_3\mathrm{Cl}}{\to }}$Y$\stackrel{\mathrm{Alk}.{\mathrm{KMnO}}_4}{\to }$Z                                     

The product Z is

1. toluene

2. benzaldehyde

3. benzoic acid

4. benzene

The compound having lowest boiling point among the following is -

1. Phenol                                 

2. o-Nitrophenol

3. m-Nitrophenol                       

4. p-Nitrophenol

The ionisation constant of phenol is higher than that of ethanol because -                   

1. Phenoxide ion is bulkier than ethoxide

2. Phenoxide ion is a stronger base than ethoxide

3. Phenoxide ion is stabilised through delocalisation

4. Phenoxide ion is less stable than ethoxide

Which represents Riemer-Tiemann reaction?

(a)
(b)
(c)
(d)

The boiling point of p-nitrophenol is higher than that of o-nitrophenol because -               

1. NO₂ group at p-position behaves in a different way from that at o-position.

2. Intramolecular hydrogen bonding exists in p-nitrophenol.

3. There is intermolecular hydrogen bonding in p-nitrophenol.

4. p-Nitrophenol has a higher molecular weight than o-nitrophenol.

Increasing order of acidic strength of

p-Methoxy phenol (I),

p-Methyl phenol (II)

 p-Nitrophenol (III)

is -                                                             

1. III, I, II             

2. II, I, III           

3. III, II, I         

4. I, II, III