/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} 41P The following names are all inco... [FREE SOLUTION] | 91Ó°ÊÓ

91Ó°ÊÓ

The following names are all incorrect or incomplete, but they represent real structures. Draw each structure and name it correctly.

(a)2-ethylpentane

(b) 3-isopropylhexane

(c) 5-chloro-4-methylhexane

(d) 2-dimethylbutane

(e) 2-cyclohexylbutane

(f)2,3-diethylcyclopentane


Short Answer

Expert verified

(a)

(b)

(c)

(d)

(e)

(f)

Step by step solution

01

Alkanes

Alkanes are hydrocarbon containing only single bonds. The general formula for alkane is CnH2n+2,where n = number of carbon atoms.

02

Rules for naming alkanes

In order for an alkane to be named, following rules must be followed.

(a) The longest continuous chain of carbon atoms is identified, which gives the base name.

(b) Starting with the end nearest a branch, the longest carbon chain is numbered.

(c) Substituents present on the longest chain, such as alkyl groups, are named, and each substituent is located by the number of the main chain carbon atoms to which it is attached.

(d) Listing is done in alphabetical order if two or more substituents are present. Prefixes like di-, tri-, tetra-, etc., are used if there are two or more of the same alkyl substituents.

03

Identifying the correct name and drawing its structure

(a)The correct name will be 3-methylhexane.

(b)The correct name will be3-ethyl-2-methylhexane.

(c)The correct name will be2-chloro-3-methylhexane.

(d)The correct name will be2,2-dimethylbutane.

(e)The correct name will bebutylcyclohexane.

(f)The correct name will be1,2-diethylcyclopentane.

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 91Ó°ÊÓ!

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

Use a Newman projection about the indicated bond to draw the most stable conformer for each compound.

(a)3-³¾±ð³Ù³ó²â±ô±è±ð²Ô³Ù²¹²Ô±ð â¶Ä‰a²ú´Ç³Ü³Ù â¶Ä‰t³ó±ð C2−°ä3 â¶Ä‰b´Ç²Ô»å

(b)3,3-»å¾±³¾±ð³Ù³ó²â±ô³ó±ð³æ²¹²Ô±ð â¶Ä‰a²ú´Ç³Ü³Ù â¶Ä‰t³ó±ð C3−°ä4 â¶Ä‰b´Ç²Ô»å

Table 3-6 shows that the axial-equatorial energy difference for methyl, ethyl, and isopropyl groups increases gradually: 7.6, 7.9 and 8.8 kJ/mol (1.8, 1.9, and 2.1 kcal/mol). The tert-butyl group jumps to an energy difference of 23 kJ/mol (5.4 kcal/mol), over twice the value for the isopropyl group. Draw pictures of the axial conformations of isopropylcyclohexane and tert-butylcyclohexane and explain why the tert-butyl substituent experiences such a large increase in axial energy over the isopropyl group.

Draw the two chair conformations of each compound, and label the substituents as axial and equatorial. In each case, determine which conformation is more stable.

(a)cis-1-ethyl-2-isopropylcyclohexane

(b)trans-1-ethyl-2-isopropylcyclohexane

(c)cis-1-ethyl-3-methylcyclohexane

(d)trans-1-ethyl-3-methylcyclohexane

(e)cis-1-ethyl-4-methylcyclohexane

(f)trans-1-ethyl-4-methylcyclohexane

In each pair of compounds, which compound has the higher boiling point? Explain your reasoning.

(a) Nonane or 3-methylheptane

(b) Octane or 2,3,4-trimethylpentane

(c) 2,3,5-trimethylhexane or nonane

Name the following alkane and haloalkane. When two or more are present list them in alphabetical order.

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.