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4. This question is in reference to Table 1 found in Section 3 "Scientific Results in Support of Thalidomide Victims." Based on the results, what can you conclude about the teratogenicity of the racemic mixture versus R/S enantiomers of thalidomide?

5. This question is in reference to Table 2 found in Section 3 "Scientific Results in Support of Thalidomide Victims." What can you conclude about the inversion rate for the two enantiomers?

6. The rate of inversion 0.5 (hr-1) corresponds to 5 inversions in one hour. How many inversions occurred an hour for thalidomide as reported in Table 2 from R to S and from S to R?

please give a detailes explanation thank you.
4. (1 pt.) This question is in reference to Table 1 found in Section 3 Scientific Results in Support of Thalidomide Victims
Table 1: Teratogenicity of the Optical Isomers of Thalidomide in New Zealand White Rabbits (based on Fabro, Smith, and Willia
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(4.) Teratogeneity Page 0 solution is the ability of a dry interfed with the development of a fetus, binth defects. On table

5. The (R)-enantiomer of Thalidomide has sedative effects, whereas the (S)-isomer is teratogenic. Now, the kRS=0.30 and kSR= 0.31 that means the rate of the S to R formation is higher than the rate of R to S formation. So, according to the inversion constant, there may be an accumulation of R isomer, but accumulation of S isomer is not possible.

6. R to S is 3 inversions in one hour

S to R is 3.1 inversions per hour

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