How can I draw the cis-1-bromo-3-methylcyclohexane chair conformation?

Answer 1

The first step in drawing the chair conformation for cis-1-bromo-3-methylcyclohexane is to analyze what cis means. The easiest way to explain what cis means is to look at the compound's wedge-dash notation.

If two groups are on a wedge, which means that they are coming out of the plane of the page, they are said to be cis, or have a cis relationship. If one of the two groups is on a wedge, and the other is on a dash (going into the plane of the page), then they are said to be trans.

Since we were told that the compound is cis, the bromo and methyl groups must either be both on a wedge, or both on a dash. I'll show you the case when both are on a wedge

Next, you have to number each carbon atom; you start from any carbon atom and go either clockwise, or counterclockwise, the only important thing is that you keep track of what carbon is numbered as (1) and what direction you used.

I'll use as carbon (1) the one that has the bromo group attached. I'll go clockwise, which means that the methyl group will be attached to carbon (3).

Now draw your chair conformation template.

Notice that the carbon atoms are numbered by going in the same clockwise direction. Now, there are two ways you can add groups to a chair conformation.

One way is UP, which is equivalent of a group that's on a wedge, and the other way is DOWN, which is equivalent ot a group that's on a dash.

SInce you're got the bromo and methyl groups in cis, both must be placed on axial bonds, or UP. Here's how that would look

The bromo group is up on carbon (1), while the methyl group is down on carbon (3). That's a chair conformation for cis-1-bromo-3-methylhexane.

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Answer 2

To draw the cis-1-bromo-3-methylcyclohexane chair conformation, follow these steps:

  1. Draw a cyclohexane ring with six carbons.
  2. Identify the position of the methyl group (CH3) and the bromine atom (Br) on the ring.
  3. Place the methyl group in the equatorial position to minimize steric hindrance.
  4. Place the bromine atom either in the axial or equatorial position, depending on the cis configuration.
  5. If the bromine and methyl groups are on the same side (cis), place the bromine in the equatorial position to minimize steric hindrance.
  6. Draw the chair conformation, ensuring that all bonds are shown accurately and the positions of the substituents are clear.

Remember to consider the stereochemistry and the stability of the chair conformation when drawing the molecule.

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Answer from HIX Tutor

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

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