A: Phenol does not react with NaHCO3 but 2,4,6-trinitrophenol does react, with the evolution of CO2
R: 2,4,6-trinitrophenol is a stronger acid than carbolic acid.
Both Assertion and Reason are true and the reason is the correct explanation of the assertion
Both Assertion and Reason are true but the reason is not the correct explanation of the assertion
Assertion is a true statement but the reason is false.
Both Assertion and Reason are false statements.
A: Picric acid is more acidic than formic acid.
R: Picric acid has three -COOH groups whereas formic acid has one -COOH group.
A: -OH, -OCH3 groups are o, p-directing.
R: Ring is activated by the resonance effect of -OH, -OCH3 groups.
Both Assertion and Reason are true and the reason is the correct explanation of the assertion.
Both Assertion and Reason are true but the reason is not the correct explanation of the assertion.
Amongst the following, the alcohol that reacts with conc. HCl /anhydrous ZnCl2 to form alkyl halide at room temperature, will be
CH3-CH2-OH
Ph-CH2-CH2-OH
Ph-C| CH3|CH3-OH
Anisole on reaction with HI gives-
The reaction between acetone and methylmagnesium chloride followed by hydrolysis will give:
sec-Butyl alcohol
tert-Butyl alcohol
iso-Butyl alcohol
iso-Propyl alcohol
Cyclohexanol gives best yield of cyclohexene with -
conc.H3PO4
conc.HCl
conc.HBr
All of the above
When benzenediazonium chloride is treated with water, the compound formed is :
C6H5COOH
C6H5OH
C6H6
C6H5NH2
Which of the following substituted phenols is the strongest acid?
Preparation of phenol from cumene is -
Reduction Reaction
Oxidation reaction
Disproportionation Reaction
Ozonolysis
The reagent used for the bromination of phenol to 2,4,6-tribromophenol is/are-
Match the structures of the compounds given in Column I with the name of the compounds given in Column II.
Column I
Column II
A.
1. Phenetole
B.
2. o-Cresol
C.
3. Catechol
D.
4. Resorcinol
Codes
A B C D
2 4 1 3
3 1 4 2
1 4 3 2
4 3 2 1
Match the starting material in Column I with the products formed (Column II) in the reaction with HI.
A. CH3-O-CH3
1.
2. CH3 |CH3-C-I+CH3OH | CH3
C. CH3 |H3C-C-O-CH3 | CH3
3.
4. CH3-OH+CH3I
5.
6.
2 3 4 1
3 1 5 2
5 4 3 2
4 5 2 1
CH3CH2CH=CH2→H2O, H2O2, OH-B2H6Z
Z in the above reaction is -
CH3CH2CH2CH2OH
CH3CH2C| OHHCH3
CH3CH2CH2CHO
CH3CH2CH2CH3
Match the items of Column I with items of Column II.
Column l
Column ll
A. Solvent used in perfumes
1. Neutral ferric chloride
B. Wood spirit
2. Glycerol
C. Reagent used for detection of phenolic group
3. Methanol
D. By product of soap industry used in cosmetics
4. Ethanol
4 3 1 2
A. Reimer-Tiemann reaction
1. Conversion of phenol to o-hydroxysalicylic aid
B. Kolbe's reaction
2. Heated copper at 573K
C. Conversion of 2° alcohol to a ketone
3. Reaction of an alkyl halide with sodium alkoxide
D. Williamson's synthesis
4. Conversion of phenol to salicylaldehyde
3 4 1 2
4 1 2 3
Assertion: The addition reaction of water to but-1-ene in acidic medium yields butan-1-ol.
Reason: Addition of water in an acidic medium proceeds through the formation of a primary carbocation.
Both Assertion and Reason are true and the Reason is the correct explanation of Assertion.
Both Assertion and Reason are true and Reason is not the correct explanation of Assertion.
Assertion is true but the Reason is false.
Both Assertion and Reason are false.
Assertion: p-Nitrophenol is more acidic than phenol.
Reason: Nitro group helps in the stabilization of the phenoxide ion by dispersal of negative charge due to resonance.
Both Assertion and Reason are true and the Reason is not the correct explanation of Assertion.
Assertion is true but the reason is false.
Assertion is false but the reason is true.
Assertion: IUPAC name of the compound
is 2-ethoxy-2-methylethane.
Reason: In IUPAC nomenclature, ether is regarded as a hydrocarbon derivative in which a hydrogen atom is replaced by —OR or —OAr group
[where, R = alkyl group and Ar = aryl group].
Assertion is false but the Reason is true.
Assertion: Bond angle in ethers is slightly less than the tetrahedral angle.
Reason: There are a repulsion between the two bulky (— R) groups.
Both assertion and Reason are true and the Reason is the correct explanation of Assertion.
Assertion is false but Reason is true.
Assertion: Boiling points of alcohols and ethers are high.
Reason: They can form intermolecular hydrogen bonding.
Assertion and Reason both are false.
Assertion: Bromination of phenol is carried out in the presence of Lewis acid.
Reason: Lewis acid polarizes the bromine molecule.
Assertion: o-Nitrophenol is less soluble in water than the m and p-isomers.
Reason: m and p-Nitrophenols exist as associated molecules.
Assertion: Ethanol is a weaker acid than phenol.
Reason: Sodium ethoxide may be prepared by the reaction of ethanol with aqueous NaOH.
Assertion: Phenol forms 2,4,6-tribromophenol on treatment with Br2, in carbon disulphide at 273K.
Reason: Bromine polarises in carbon disulphide.
Assertion and Reason both are false
Assertion: Phenols give o-and p-nitrophenol on nitration with conc. HNO3 and H2SO4 mixture.
Reason: —OH group in phenol is o-, p-directing.
The number of structural isomers of alcohol of formula C5H12O are -
4
6
8
10
The number of monohydric phenols that can have the molecular formula, C7H8O are-
2
3
5
If chlorobenzene is treated with A. NaOH and B. HCl
The final product formed is :
Benzamide
Phenol
Cumene
Benzoic acid
Phenol is more acidic than ethanol due to -
Resonance
Phenoxide ions
Less -I effect
More ability to gain a proton
Please disable the adBlock and continue. Thank you.