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Classification of Alcohols and Ethers

by shruti · shared 29 days ago
10
Questions
~6m
To complete
0
Times taken
Organic Chemistry
Subject
Deck intelligence

What this deck covers

Focus
Organic Chemistry
Practice shape
Quick check
Question mix
4 multiple choice · 6 written
Coverage
12 study sections
AlcoholsEthersIupac NomenclaturePhenolsDehydration MechanismFunctional Groups
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Sneak peek · question 1

How are ethers classified according to the structure of their alkyl groups?

4 choices · multiple choice
    Question 02

    How is the name of a polyhydric alcohol constructed according to the IUPAC naming system?

    Question 03

    What type of groups do ethers contain according to IUPAC nomenclature?

    Question 04

    What is one method by which phenol is obtained from chlorobenzene?

    • A)
      By acidification of sodium phenoxide
    • B)
      By oxidation of isopropylbenzene
    • C)
      By reacting benzene with nitrous acid
    • D)
      By heating benzene sulphonic acid
    Question 05

    What are the steps involved in the mechanism of dehydration of ethanol?

    Question 06

    What reagent is used to oxidize primary alcohols to aldehydes with good yield?

    Question 07

    Why do ethers have boiling points that are much lower than those of alcohols?

    • A)
      Due to the presence of hydrogen bonding in ethers
    • B)
      Because ethers have a weak polarity
    • C)
      Because ethers do not form hydrogen bonds
    • D)
      Due to the absence of alkyl groups in ethers
    Question 08

    What catalyst is used in the Friedel-Crafts reaction involving anisole?

    Question 09

    How are alcohols and phenols classified according to the carbon atom's hybridization?

    Question 10

    What is one reaction that demonstrates the acidic nature of phenol?

    • A)
      The reaction of phenol with sodium bicarbonate
    • B)
      The reaction of phenol with sodium hydroxide
    • C)
      The reaction of phenol with dilute hydrochloric acid
    • D)
      The reaction of phenol with sodium metal