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2. Chemistry
3. Alcohols,Phenols and Ethers
4. NCERT Exercise Based MCQs (44 Qs)
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Select Chapter Topics:Alcohols: Preparation & PropertiesMechanism of Dehydration, Methanol & EthanolPhenols: Preparation & PropertiesElectrophilic Substitution Reactions, Uses of PhenolsEthers: Preparation & Properties, Uses

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Q. No.Q13:

An appropriate set of reactants for the preparation of 1-methoxy-4-nitrobenzene is/are :

1.
2.
3.	\(\mathrm{CH_3-CH_2-CH_2-O-CH_3+HBr}\)
4.	\(\mathrm{(CH_3)_3C-OC_2H_5+HI}\)

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4-Methoxytoluene will be the major product in : 1. Friedel-Crafts reaction-alkylation of anisole 2. Nitration of anisole 3. Bromination of anisole in ethanoic acid medium 4. Friedel-Craft’s acetylation of anisole

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The alkoxy group in aryl alkyl ethers activates the benzene ring towards:

1. Nucleophilic addition reaction

2. Electrophilic addition reaction

3. Nucleophilic substitution reaction

4. Electrophilic substitution reaction

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1.	1-Propoxypropane	2.	2-Propoxypropane
3.	1-Propoxyethane	4.	2-Ethoxypropane

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The preferred alkyl halide for the synthesis of ether in Williamson synthesis is:

1.	Secondary	2.	Tertiary and secondary both
3.	Tertiary	4.	Primary

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The compound having the lowest boiling point is:

1.	Ethanol	2.	Methanol
3.	Methoxymethane	4.	Propanol

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Potassium permanganate reagent is used for : 1. Oxidation of primary alcohol to carboxylic acid. 2. Oxidation of primary alcohol to aldehyde. 3. Bromination of phenol to 2,4,6-tribromophenol. 4. Dehydration of propan-2-ol to propene.

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1.	Propene → Propan-2-ol
2.	Benzyl chloride → Benzyl alcohol
3.	Ethyl magnesium chloride → Propan-1-ol
4.	Ethanol →Ethene

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The group that activates the benzene ring towards electrophilic substitution reaction is:

1.	OH	2.	NO2
3.	CN	4.	COOH

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Phenol is more acidic than ethanol due to:

1. Resonance

2. Phenoxide ions

3. Less -I effect

4. More ability to gain a proton

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