Concept explainers
(a)
Interpretation:
1,3-dimethylcyclopentane showing cis-trans isomerism to be identified.
Concept Introduction:
For getting cis trans isomerism atleast two substituent need to be attached with the parent cyclic chain of carbon.
The cis isomer indicates the position of substituent on same plane.
The trans isomer indicates the position of substituent are on opposite plane.
(b)
Interpretation:
Ethylcyclopentane showing cis-trans isomerism to be identified.
Concept Introduction:
For getting cis trans isomerism atleast two substituent need to be attached with the parent cyclic chain of carbon.
The cis isomer indicates the position of substituent on same plane.
The trans isomer indicates the position of substituent are on opposite plane.
(c)
Interpretation:
1,3- dimethylcyclohexane showing cis-trans isomerism to be identified.
Concept Introduction:
For getting cis trans isomerism atleast two substituent need to be attached with the parent cyclic chain of carbon.
The cis isomer indicates the position of substituent on same plane.
The trans isomer indicates the position of substituent are on opposite plane.
Want to see the full answer?
Check out a sample textbook solutionChapter 11 Solutions
INTRO.TO GENERAL,ORGAN...-OWLV2 ACCESS
- correct option is 2 I know explaain why it is also I need explaination why other options 1 3 & 4 are incorrect (along with structures) if u won't explaain like this manner I will. downvote for surearrow_forwardPractice git#t ų Give IUPAC names for the following molecules a) F- b) Farrow_forwardPROBLEM 3-25 (a) Draw both chair conformations of cis-1,4-dimethylcyclohexane, and determine which conformer is more stable. (b) Repeat for the trans isomer. (c) Predict which isomer (cis or trans) is more stable.arrow_forward
- PROBLEM 3-5 All of the following names are incorrect or incomplete. In each case, draw the structure (or a possible structure) and name it correctly. (a) 2-methylethylpentane (c) 3-dimethylhexane (e) 2-bromo-3-ethylbutane (b) 2-ethyl-3-methylpentane (d) 4-isobutylheptane (f) 2-diethyl-3-methylhexanearrow_forwardPROBLEM 3-3 Write structures for the following compounds. (a) 3-ethyl-4-methylhexane (b) (d) (c) 4-tert-butyl-2-methylheptane 3-ethyl-5-isobutyl-3-methylnonane 5-isopropyl-3,3,4-trimethyloctanearrow_forward[References] The compounds shown here consist of a cyclohexane ring, a methyl group, and a hydroxyl group. Which one shows cis-trans isomerism but has no stereocenters? CH3 OH HO CH₂ Submit Answer Try Another Version 1 item attempt remainingarrow_forward
- what is the iupac names for each cycloalkanes?arrow_forwardProblem 10-3 For each molecular formula, draw all the possible constitutional isomers of alcohols with that formula. Give the IUPAC name for each alcohol. a. C3H8O b. C4H100 C. C₂HO d. C3H4Oarrow_forwardPractice Draw the structure of the following compounds. 1. bicyclo [4.2.1]nona-4,7-dien-2-ol 2. 5-bromo-7,7-dimethylbicyclo [2.2.1]heptan-2-one 3. 3-chloro-2,5-dimethylbicyclo[4.3.0]nonan-8-one 4. 6-ethoxy-1,2-dimethylspiro [2.4]heptane-5-carbaldehydearrow_forward
- PROBLEM 3-24 Draw the most stable conformation of: (a) ethylcyclohexane (c) cis-1-tert-butyl-4-isopropylcyclohexane (b) 3-isopropyl-1, 1-dimethylcyclohexanearrow_forwardProblem 11-4 Write the molecular formula and IUPAC name for each alkane.arrow_forwardPROBLEM 3-11 huon Give IUPAC names for the following compounds: (a) The three isomers of C5H12 (b) (c) CH3 (CH3)2CHCH₂CHCH3 (d) CH3 1 CH3CH₂CHCHCH3 CH3 CH3 (CH3)3CCH₂CH₂CH CH3arrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning