Phenols does not react with

Phenols does not react with
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Phenols does not react with A. sodium bicarbonate B. sodium hydroxide C. potassium hydroxide D. ferric chloride
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Explain why nucleophilic substitution reactions are not very common in phenols.

Description : Explain why nucleophilic substitution reactions are not very common in phenols.

Last Answer : Explain why nucleophilic substitution reactions are not very common in phenols.

Assertion : Phenols are more acidic than aliphatic alcohols. Reason : Phenoxides are stabilized by resonance.

Description : Assertion : Phenols are more acidic than aliphatic alcohols. Reason : Phenoxides are stabilized by resonance.

Last Answer : Assertion : Phenols are more acidic than aliphatic alcohols. Reason : Phenoxides are stabilized by resonance. ... D. A is incorrect but R is correct

Assertion (A): Alkyl aryl ethers on reaction with HI give alkyl iodide phenols Reason (R): Aryl - oxygen bond is weaker than alkyl oxygen bond

Description : Assertion (A): Alkyl aryl ethers on reaction with HI give alkyl iodide phenols Reason (R): Aryl - oxygen bond is weaker than alkyl oxygen bond

Last Answer : Assertion (A): Alkyl aryl ethers on reaction with HI give alkyl iodide phenols Reason (R): Aryl - oxygen ... is false D. A is false but R is true

The smell of fat turned rancid is due to (A) Presence of vit E (B) Presence of quinones (C) Phenols (D) Volatile fatty acids

Description : The smell of fat turned rancid is due to (A) Presence of vit E (B) Presence of quinones (C) Phenols (D) Volatile fatty acids

Last Answer : Answer : D

Protein is a polymer of (A) Sugars (B) Phenols (C) Amino acids (D) Carboxylic acids

Description : Protein is a polymer of (A) Sugars (B) Phenols (C) Amino acids (D) Carboxylic acids

Last Answer : Answer : C

Phenols are added in gasoline to (A) Improve the octane number(B) Act as an antioxidant(C) Reduce its viscosity(D) Increase its pour point

Description : Phenols are added in gasoline to (A) Improve the octane number (B) Act as an antioxidant (C) Reduce its viscosity (D) Increase its pour point

Last Answer : (B) Act as an antioxidant

Phenols do not undergo substitution of the — OH group like alcohols. Explain.

Description : Phenols do not undergo substitution of the — OH group like alcohols. Explain.

Last Answer : The C — O bond in phenols has some double bond character due to resonance and hence cannot be easily cleaved by a nucleophile. In contrast, the C — O bond in alcohols is a pure single bond and hence can be easily cleaved by a nucleo phile.

While separating a mixture of ortho and para-nitro phenols by steam distillation, name the isomer which will be steam volatile. Give reasons.

Description : While separating a mixture of ortho and para-nitro phenols by steam distillation, name the isomer which will be steam volatile. Give reasons.

Last Answer : In o-nitrophenol, there is intramolecular hydrogen bonding as follows : In p-nitrophenol, there is intramolecular hydrogen bonding as follows :   Due to intermolecular H ... -nitrophenol. Hence o-nitraphenol due to its lower b. p. is steam volatile while pnitrophenol is not.

Alcohols are easily protonated than phenols. Justify.

Description : Alcohols are easily protonated than phenols. Justify.

Last Answer : Ans. In phenols lone pair of electrons on the oxygen atom are delocalised over the benzene ring due to resonance and hence are not easily available for protonation. In contrast in alcohols, ... oxygen atom are localized due to absence of resonance and hence are easily available for protonation. 

Phenol has smaller dipole moment than methanol. (OR) Why are dipole moments of phenols smaller than dipole moments of alcohols ?

Description : Phenol has smaller dipole moment than methanol. (OR) Why are dipole moments of phenols smaller than dipole moments of alcohols ?

Last Answer : Due to electron-withdrawing effect of the benzene ring, the C — O bond in phenol is less polar but in case of methanol due to electron-donating effect of — CH3 group, C — O bond is more polar.

Phenols can be easily distinguished from alcohols because (a) phenols are soluble in NaOH, but alcohols are not (b) alcohols are soluble in NaOH, but phenols are not (c) phenols are soluble in NaHCO3, but alcohols are not (d) alcohols are soluble in NaHCO3, but phenols are not

Description : Phenols can be easily distinguished from alcohols because (a) phenols are soluble in NaOH, but alcohols are not (b) alcohols are soluble in NaOH, but phenols are not (c) phenols are soluble in NaHCO3, but alcohols are not (d) alcohols are soluble in NaHCO3, but phenols are not

Last Answer : phenols are soluble in NaOH, but alcohols are not

Which group forms the strongest H-bonds to water molecules? (a) Alcohols (b) Ethers (c) Phenols (d) All equally strong

Description : Which group forms the strongest H-bonds to water molecules? (a) Alcohols (b) Ethers (c) Phenols (d) All equally strong

Last Answer : Phenols

Which one of the following compounds form zwitterions?(a) carbonyl compounds (b) amino acids (c) phenols (d) heterocyclic compounds

Description : Which one of the following compounds form zwitterions? (a) carbonyl compounds (b) amino acids (c) phenols (d) heterocyclic compounds

Last Answer : amino acids