Isomers - Organic Chemistry

A stereocenter exists when the central atom is bound to four unique substituents. In the given molecule, the carbons are numbers from left to right. Carbons 1, 3, 5, 6, and 8 are all bound to at least two hydrogen atoms and cannot be stereocenters. Similarly, the carbons in the two methyl groups (bound to C4 and C7) do not qualify as stereocenters. Carbon 7 has two identical methyl substituents. This leaves only C2 and C4. The molecule has two stereocenters.

Carboxylic acid is highest priority, so carbon chain labelled from right to left. Since highest priority groups are on the same side of the double bond, it's given the "Z" designation.

The molecules in this problem are isomers because they each have unique configurations and do not share the same funcitonal groups at the same carbon positions. Enantiomers are reflections of each other. Diastereomers are stereoisomers that differ at one or more stereocenters, while epimers are stereoisomers that differ at only one stereocenter.

There are four unique constitutional isomers possible for the given formula; meaning that they may not be made identical by conformational changes. They are illustrated as follows:

The most favorable chair conformation of a six-member ring is that in which the greatest number of large substituents are oriented equatorially. Conformation I corresponds to the given Haworth projection and orients all three large substituents in equatorial positions, making it the least energetic (most favorable) conformation.

The two given molecules are conformational isomers. The molecules are superimposable by horizontally rotating either structure 180 degrees and rotating the bond between carbons 2 and 3. Both enantiomers and diastereomers are non-superimposable and constitutional isomers must have non-configurational differences in structure. There is no internal plane of symmetry, thus neither compound can be meso.

Based on the Haworth projection given, the relative orientations of the three substituents are bromine up, hydroxide: down, hydroxide: up. In the most stable chair conformation, the largest substituents are oriented equatorial. If bromine is oriented equatorial up, the hydroxide at carbon 2 is equatorial down and the hydroxide at carbon 4 is axial up.

The anti conformation is most stable in a Newman projection because this is the form where the two largest functional groups are facing opposite directions and are furthest away from each other. However, note that in rare cases, such as in 1,2-ethandiol, the gauche conformation is more stable due to intramolecular hydrogen bonding. All other conformations have the functional groups closer to each other causing some repulsion and instability. The least stable of them all is the eclipsed conformation because this is the form where the functional groups are closest to each other.

In a Fischer projection, the groups on the left and right are coming out of the screen and towards the viewer. On the other hand, the top and bottom groups are going into the screen away from the viewer. One way to help you remember this is to think of the Fischer projection as a skeleton wearing one or more bowties (the skeleton is vertical and its bonds are drawn as dashes, which are going into the plane of the page/screen, and the horizontal bonds are drawn as wedges, which are coming out of the plane of the page/screen).

The given images are Fisher projections of the molecules. To compare them, we must mentally rotate the substituents around the carbon-carbon bond through the molecule's center, as well as consider flipping the projection end-over-end.

If the molecule to the left were flipped directly end-over-end, it will match the molecule to the right, with the methyl pointed upward in the front plane and the ethyl pointed downward in the rear plane. These molecules are identical.

The molecules shown contain three stereocenters as evidenced by the bonds of carbons 2, 3, and 4 to four unique groups. Rotating the molecule on the right 180 degrees in the horizontal plane reveals that only carbon 2 differs in absolute configuration (R/S). As a general rule, switching the absolute configurations of all stereocenters present in a compound yields its enantiomer. Switching the configuration at least one stereocenter, but not all, yields diastereomers, non-superimposable stereoisomers that are not mirror images. The two molecules shown are diastereomers. A molecular modeling kit can prove extremely useful in visualizing the difference in such situations.

Carbon 1 is not a stereocenter as both constituents on the carbon are identical. For carbon 2, the bromine is the attachment with the most priority, followed by carbon 3, then carbon 1. Because bromine is in the back, the stereocenter is designated as an S. For carbon 3, the alcohol group is the attachment with the most priority, followed by carbon 2, then carbon 4. Because alcohol is in the front, the stereocenter is designated as an S.

To label each stereocenter as R or S, we must use the Cahn-Ingold-Prelog priority system.

Lets start with stereocenter 1: The is given first priority because it is the most massive constituent. The carbon to the right is given second priority because it is closer to the alcohol group and the carbon to the left is given third priority. These atoms lay clockwise by priority. However, because the hydrogen (not depicted) is in the front, we know that the stereocenter should be labeled as S.

Stereocenter 2: The is given first priority. The carbon on top is given second priority while the carbon on the bottom is given third priority. These atoms lay counterclockwise by priority. Because the hydrogen (not depicted) already faces toward the rear, we know that the steroecenter should be labeled as S.

To find the number of stereo isomers in a given molecule, we must count the number of stereocenters first.

(indicated by red dots)

Then, use the formula to get the number of stereoisomers ( being the number of stereocenters).

Corresponding stereoisomers differ in biological properties. The inversion of just one stereocenter on a large, complex molecule can alter the biological properties of the entire molecule. All other statements are true.

To find the number of diastereomers, we must first find the number of stereocenters, then the number of stereoisomers. The stereocenters are the carbon atoms with the red dots next to them, we have three:

To find the number of stereoisomers, we use the formula , where is the number of stereocenters. We have 8 stereoisomers. Finally, the definition of a diastereomer is a stereoisomer that is not an enantiomer. Optically active molecules have only one enantiomer, so that leaves us with 7 remaining diastereomers (including the original molecule itself).

There are 4 chiral carbons on the molecule shown below:

The number of stereoisomers for a given molecule = 2n where n equals the number of chiral centers (in this case 4). Also there are no internal planes of symmetry, so there is no possibility for meso compounds.

The following products are a mix of constitutional isomers and stereoisomers.

The correct answer is 2 stereoisomers. To determine the number of stereoisomers that a compound may be present in, the number of stereocenters must be determined. In the case of methylcyclopropane, we have only one stereocenter, which is the carbon in the ring that is bound to the methyl group. Once the number of stereocenters is determined, we can use the following formula to determine the number of stereoisomers:

Where is equal to the number of stereocenters. Therefore,

If a molecule has n sterocenters, it has up to possible steroisomers. Thus, the given molecule has or possible stereoisomers. Keep in mind the key word here is maximum, where the molecule may have less than 32 steroisomers, for instance when discussing meso compounds.