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 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,
PhenolXYZ
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?
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