Question: Give both the IUPAC name and the common name for each alcohol.

(a)

(b)

(c)

(d)

Short Answer

Expert verified

Answer

(a)The IUPAC name of the compound is propan-2-ol.

The common name of the compound is isopropyl alcohol.

(b)The IUPAC name of the compound is cyclobutanol.

The common name of the compound is cyclobutyl alcohol.

(c)The IUPAC name of the compound is 1-cyclopropylpropan-1-ol.

The common name of the compound is 1-cyclopropylpropan-1-ol.

(d)The IUPAC name of the compound is 2-methylpropan-1-ol.

The common name of the compound is isobutyl alcohol.

Step by step solution

01

IUPAC name of alcohols

The longest chain comprising the carbon atom is named first during the compound naming. A suffix of –ol is provided to name alcohols. The hydroxyl groups include greater preference than the double and triple bonds.

02

Common name

The common name of particular alcohol is acquired from the alkyl group’s common name and the term alcohol. IUPAC names are common names if the molecule possesses a complex structure.

03

Identifying the IUPAC name and common name of each alcohol

(a) The longest carbon chain comprises three carbon atoms and is saturated in the given compound. So the carbon chain is propane. The OH group is found at the second carbon.

Hence, remove –e from propane and add –ol as the suffix. Since the –OH group is on the second carbon, the compound’s name is propan-2-ol.

The naming of compound A

The IUPAC name of the compound is propan-2-ol.

The common name of the compound is isopropyl alcohol.

(b) In the given compound, the longest chain comprises four carbon atoms in the form of a ring. So the carbon chain is cyclobutane. The OH group is found at the first carbon atom. Hence, the name of the compound is cyclobutanol.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Draw the structures of the following compounds. (Includes both new and old names.)

(a) diphenylmethanol

(b) 3-(chloromethyl)heptan-3-ol

(c) 3-cyclohexen-1-ol

(d) 3-cyclopentylhexan-2-ol

(e) meso-3,5-heptanediol

(f) cyclohexene glycol

(g) 3-(bromomethyl)phenol

(h) (2R,3R)-2,3-pentanediol

(i) cyclohex-3-ene-1-thiol

(j) diethyl disulfide

(k) 2-methylhex-4-yn-2-ol

A nitro group (-NO2) effectively stabilizes a negative charge on an adjacent carbon atom through resonance:

Two of the following nitrophenols are much more acidic than phenol itself. The third compound is only slightly more acidic than phenol. Use resonance structures of the appropriate phenoxide ions to show why two of these anions should be unusually stable.

Arrange the following compounds in order of decreasing acidity.

CH3COOH CH3OH CH3CH3 CH3SO3H CH3NH2 CH3SH CH3CCH

Show how you would synthesize the following compounds from alkyl halides, vinyl halides, and aryl halides containing no more than six carbon atoms.

  1. octane
  2. vinylcyclohexane
  3. trans-oct-3-ene
  4. cyclopentyl propyl ketone

Ever since the Grignard reaction was discovered to react with ethylene oxide, chemists have experimented with other epoxides to test the limits of this reaction (which chemists call the scope of the reaction). The conclusion is that the success of the Grignard reaction is limited by the steric hindrance in the epoxide. One group published results of several Grignard reagents on one epoxide; one of their products is shown here. What Grignard reagent and what epoxide were used to make this compound? Comment on the steric requirements of the epoxide and the stereochemistry of the product.

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free