4. For the two compounds below, add the missing chlorine atom to the appropriate carbon atom (1,4 or 1,2) and attachin the appropriate cis or trans fashion.trans-1-bromo-4-chlorocyclohexanecis-1-bromo-2-chlorocyclohexaneBrBr-add the chlorine atomadd the chlorine atomOnce drawn, state the number of axial and equatorial hydrogen atoms are on each ring.number of axial H-atoms:number of axial H-atoms:number of equatorial H-atoms:number of equatorial H-atoms:

The missed chlorine atoms in both the given strictures are identified and drawn in step two.

Answered: 4. For the two compounds below, add the…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter7: Cycloalkanes

Section: Chapter Questions

Problem 2CTQ

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Similar questions

A 1, 2-cis disubstituted cyclohexane, such as cis-1, 2-dichlorocyclohexane, must have one group axial and one group equatorial. Explain.
Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This group is called an ethyl group and can be considered a sphere about twice the sizeof a methyl group. Draw the following Newman projections sighting down the C1C2 bond... a. The lowest potential energy conformation. b. The highest potential energy staggered conformation.
Consider the Newman projection below. a. Draw a full Lewis structure of this molecule with R1=Me,R2=Et , and R3=iPr . b. Given the sizes of these R groups (R3R2R1) , does the Newman projection above show thelowest potential energy conformation of this bond? If not, draw a Newman projectionshowing the lowest P.E. conformation (sighting down this same bond). c. To draw a Newman projection in the lowest P.E. conformation, the following rule of thumbusually applies: Place the largest group on the front carbon anti to the largest group on theback carbon. Is your answer to the previous question consistent with this rule of thumb?
Complete the Newman projection below to draw the most stable conformation of 3-methylpentane, looking down the C2-C3 bond. Identify each substituent using "H" for hydrogen and "Me" for methyl. a= b= c= d=
Imagine that this worksheet has sucked you the plane of the page, and you are now facing the indicated bond of the drawn molecule. a. Draw the six main Newman projections for the indicated bond: three eclipsed, three staggered. b. Label which conformers are eclipsed ands taggered.c. Identify the most and least stable conformer, and explain your reasoning.
Following is a staggered conformation for one of the enantiomers of 2-butanol Q. viewed along the bond between carbons 2 and 3, draw a Newman projection for this staggered conformation.
translate the bond-line notation structure to the Newman projection by filling int the missing groups (A, B, C, D or E) on the lines in the Newman projection so they match the conformation given in the original structure. Circle if the conformation is a staggered or eclipsed.
The unsaturation number or degree of unsaturation (U) can be used to determine the number of rings and multiple bonds in a compound from its molecular formula. Given a structure, you can determine the number of hydrogens without having to count them explicitly. Consider three compounds and their degree of unsaturation. (a) A compound A has the molecular formula C7H13ClN2OC7⁢H13⁢ClN2O. How many rings and/or π bonds does it contain?
a. For each disubstituted cyclohexane below, draw its ring-flip isomer. Circle the most stable conformation and label the substituent groups as axial or equatorial. ( see image) b.Draw and name the seven constitutional isomers (all contain a ring of some size) for cycloalkane, C6H12.
1.1 Build a model for line structure and use the template given to draw a Newman projection for this conformation of the compound when viewed along the C2-C3 bond. (template given in second photo) 1.2 why is this the most stable structure?
draw double-newman projection for 1. neopentane, 2. isobutyl bromide, 3. sec-butylcyclopentane, 4. trans-1,2-dichlorocyclopropane.
Illsutrate the Ring-flipping interconverts axial and equatorial hydrogens incyclohexane ?

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