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Organic 8 Online
OpenStudy (anonymous):

A trisubstituted cyclohexane compound is given below in its chair conformation. Draw the corresponding planar (overhead) representation, using wedge-and-dash bonds to indicate the substituent positions. To be graded properly, include the hydrogen atoms on the chirality centers (asymmetric carbons). Be sure that both wedge/dash bonds are drawn on the outside of the ring, or else the stereochemistry may be interpreted as square planar.

OpenStudy (photon336):

@sharmar25 what is the compound's name

OpenStudy (anonymous):

OpenStudy (photon336):

great, do you know what axial and equatorial mean?

OpenStudy (anonymous):

yes

OpenStudy (photon336):

ok do you know how to go from chair form to the ring?

OpenStudy (anonymous):

i do. I am having trouble with where the hydrogens go.

OpenStudy (photon336):

I will start by showing you how to go from chair form to the ring

OpenStudy (photon336):

Okay so the first thing, is that a dashed line means that the group is away from you, and a wedge means that the group is pointing straight at you. |dw:1441924577768:dw|

OpenStudy (photon336):

When you have your chair form you MUST number the carbons

OpenStudy (anonymous):

ok. I understand. this is what i have so far.

OpenStudy (photon336):

Number your carbons and draw the chair form like this. it is important to note whether the groups are up or down. up = wedge on your cyclohexane ring, down = dash |dw:1441924908351:dw|

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