Fischer projection is the two-dimensional representation of an organic molecule that has three dimensions. The application of this is to display a stereo formula in two dimensions in such a way that the stereochemical information of that molecule is not destroyed. The stereochemical information includes the absolute configuration of the chiral centres. It was first devised by Emil Fischer in 1891.
These projections were particularly used in the fields of chemistry and biochemistry to depict the structures of carbohydrates and amino acids. These are drawn in such a way that the chiral centre is present on the plane of the paper. Then, the two bonds are horizontally planed and are coming out of the paper whereas the other two bonds are going into the plane and are vertically planed.
How would you produce a Fischer Projection beginning with a three-
Fischer projection of D-glucose Haworth (cyclic) formulas α
i. draw the Fischer projection for each carbohydrate below ii
D-allose is an aldohexose in which all four chiral centers
Draw a Fischer projection for each of the following compounds:
Identify the two aldohexoses that will undergo a Wohl degradation to yield
Draw a Fischer Projection formula for each of the following compounds.
Determine whether each statement is true or false: a.
Draw a Fischer projection for each of the following amino acids:
Draw a Fischer projection for each of the following compounds, placing
