Which of the following is true regarding 50/50 mixture of the following molecules?

C. Smelling Chirality. Carvone Olfactory receptors in our noses, used for the detection of odors, are chiral. Therefore, in some cases, we can tell the difference between enantiomers by their odor. Carvone is one such compound that we can distinguish between the R and S enantiomer by their odor. 1. Identify the chiral center in carvone and draw the R and S enantiomers in the indicated boxes. 2. Smell both of the enantiomers of carvone and provide a brief description of their odors in the same boxes. Carvone is perfectly safe to smell as both enantiomers are found in various foods. R-carvone S-carvone

Convert the ball-and-stick model to a Fischer projection

What is the relationship between the following two molecules? a) Same molecule Ob) Enantiomers Oc) Diastereomers Structure A d) None of the above Structure B

There are nine constitutional isomers of molecular formula C7H16. 1) What is the unsaturation number of each of these compounds? 2) Draw five constitutional isomers, where two of these are chiral compounds. 3) For the three achiral constitutional isomers, provide the correct IUPAC names. 4) For the two chiral constitutional isomers, draw in Fischer projection formula the enantiomers of each. 5) Name, according to IUPAC standards, each of the enantiomers you drew in #4 above.

How many sp3 stereocenters and diastereomers(2n) does Miglitol have?

Draw the mirror image in Fischer Projection ("flat representation").