Which molecule(s) can exist as cis and trans isomers? Choose more than one answer if appropriate.Answer is D) 1,2-dimethylcyclopentaneCan you explain to me that why is the 1,2-dimethylcyclopentane? +.34) which molecule(s) can exist as cis and trans isomers?Choose more than one answer if appropriate.a) 1,1-dimethylcyclopentaneb) methylcyclopentanec) cyclopentaned) 1,2-dimethylcyclopentane

we have to select the molecule that shows cis trans isomerism

Answered: +.34) which molecule(s) can exist as…

+.34) which molecule(s) can exist as cis ana trans isomers? Choose more than one answer if appropriate. a) 1,1-dimethylcyclopentane b) methylcyclopentane c) cyclopentane d) 1,2-dimethylcyclopentane

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterNW1: Nomenclature Worksheet 1: Naming Alkanes & Cycloalkanes

Section: Chapter Questions

Problem 20CTQ: For mono-substituted cycloalkanes the “1” is not included. That is, the name1-methylcyclohexane is...

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Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

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Which molecule(s) can exist as cis and trans isomers? Choose more than one answer if appropriate.

Answer is D) 1,2-dimethylcyclopentane

Can you explain to me that why is the 1,2-dimethylcyclopentane?

+.34) which molecule(s) can exist as cis and trans isomers?
Choose more than one answer if appropriate.
a) 1,1-dimethylcyclopentane
b) methylcyclopentane
c) cyclopentane
d) 1,2-dimethylcyclopentane

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Hello, I was reading an answer from the book Organic Chemistry by Brown et al. The question is 2.51 "Draw alternative chair conformations for each substituted cyclohexane and state which chair is more stable." There are then 4 cyclohexanes (labeled a-d). For the "a" cyclohexane, the substituents are arranged as a combination of axial and equatorial in both chair conformations. However, for the "b," "c," and "d," cyclohexanes one chair has only equatorial substituents, and the other chair has only axial substituents. Why is the "a" chair conformation different? https://www.bartleby.com/solution-answer/chapter-2-problem-251p-organic-chemistry-8th-edition/9781305580350/draw-alternative-chair-conformations-for-each-substituted-cyclohexane-and-state-which-chair-is-more/4532cd91-c341-11e9-8385-02ee952b546e
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