Interpretation:
The
Concept introduction:
The anti and gauche bonds in cyclohexane are represented by sawhorse projections of staggered conformations of
The substituents in anti-relationship are
The substituents in gauche relationship are
In the following structure, each path shows anti relationship where a substituent is equatorial.
In the following structure, each path shows gauche relationship where a substituent is axial.
The torsion (dihedral) angle for eclipsed conformation is
The torsion (dihedral) angle for gauche conformation is
The torsion (dihedral) angle for anti-conformation is
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ORGANIC CHEMISTRY-PACKAGE >CUSTOM<
- Tell whether the following pairs of compounds are identical, constitutional isomers, stereoisomers, or unrelated. (a) cis-1, 3-Dibromocyclohexane and trans-1, 4-dibromocyclohexane (b) 2, 3-Dimethylhexane and 2, 3, 3-trimethy1pentanearrow_forwardFollowing is a chair conformation of cyclohexane with the carbon atoms numbered 1 through 6. (a) Draw hydrogen atoms that are above the plane of the ring on carbons 1 and 2 and below the plane of the ring on carbon 4. (b) Which of these hydrogens are equatorial? Which are axial? (c) Draw the alternative chair conformation. Which hydrogens are equatorial? Which are axial? Which are above the plane of the ring? Which are below it?arrow_forwardIdentify each substituent in the following compound as axial or equatorial, and tell whether the conformation shown is the more stable or less stable chair form (green = Cl):arrow_forward
- Me 11 H 7 H Et H a) If a substituent is placed at C-11 in the equatorial position, is this substituent cis or trans to the methyl group? b) If a substituent is placed at C-7 in the axial position, is this substituent cis or trans to the ethyl group? c) If a substituent is placed at C-1 trans to the methyl group, is this substituent axial equatorial?arrow_forwardConstruct a qualitative potential energy diagram for rotation about C-C bond of 1,2-dibromoethan. Which conformation would you expect to be more stable? label the anti and gauche conformation of 1,2-dibromoethanearrow_forwardUse valence-shell electron-pair repulsion (VSEPR) model to predict the bond angle for each of the following highlighted carbon atoms. (a) (b) -CH2OH (c) HC c- -CH=CH2 (d) (a) red carbon blue carbon (b) red carbon (c) red carbon blue carbon (d) red carbonarrow_forward
- DII F3 Provide the correct IUPAC name for the compound shown here. x F4 4, F5 O= CI-C-CH₂-CH₂-CH3 Question 8 of 20 2- 5- tert- 小 6- F6 () 3- sec- tri iso cyclo di chloro eth pent but prop chlor OIC acid oyl yl an ide 4- F7 W PrtScn F8 Home 4 F9 End F10 PgUparrow_forwardorganic chemistryarrow_forwardDraw the most stable structure of cis-1-tbutyl-2-methylcyclohexane. Your structure should clearly distinguish between axial and equatorial positions.arrow_forward
- kindly help me with this problem thank you :)arrow_forwardGiven the following partial structure, add a substituent X to C-1 so that it satisfies the indicated stereochemical requirement. What is the A -C - C - X torsion (dihedral) angle in each?arrow_forwardIn which chair conformation (a or b) is the methyl group farthest from the neighboring hydrogen atom? In which chair conformation (a or b) does the methyl group have greater room? Which is the preferred conformation of methylcyclohexane (a or b)?arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning