Organic Chemistry : Isomers
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Example Questions
Example Question #1 : Help With Comformers
Determine the most stable chair conformation corresponding to the given Haworth projection.
More than one of these
IV
II
I
III
I
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.
Example Question #71 : Isomers
How many constitutional isomers exist for the general molecular formula 
Three
Six
Four
Five
Four
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:
Example Question #72 : Isomers
In general, what is the most stable orientation in a Newman projection?
They are all equally stable
Eclipsed
Anti
Totally eclipsed
Gauche
Anti
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.
Example Question #92 : Stereochemistry
In regards to the Fischer projection shown, how are the hydroxide groups oriented?
Both are going into the screen
The left one is going into the screen and the right one is coming out
Both are lying flat in the plane of the screen
The right one is going into the screen and the left one is coming out
Both are coming out of the screen
Both are coming out of the screen
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).
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