Question 1
second option will be correct. It is because epoxidation normally chooses the side with less steric hindrance. So X = tertiary butyl group have highest steric hindrance in the given options. So apoxidation happens in the opposite direction of X. So given steriochemical outcome of the product is obtained more likely when X= tertiary butyl group.
Question 2
Third option will be correct. Substitution at A will give more steric hindrance for apoxidation compared to substitution at other two positions B and C. So substitution at A will result in the given product.
Question 3
When the two reagents are achiral then the product will be racemic mixture. That is 50-50 mixture of two enantiomers. That means racial mixture of stereoisomers.
Question 4
True
Which of the following substituents will have a greater influence on shown below? the s x-...
Part 1-Please answer the following essay questions 1. We discussed the advantages and disadvantages of internal recruiting, interviews and reference checks (and the entire hiring process). Please identify ONE disadvantage of each of these three activities -- and explain why you believe they are "disadvantages." 2. Choose ONE interview question listed below and answer it on paper as if it was being asked of you in a face-to-face interview. Please identify the Interview Question #. Details, details, details are necessary...
All of the following questions are in relation to the following journal article which is available on Moodle: Parr CL, Magnus MC, Karlstad O, Holvik K, Lund-Blix NA, Jaugen M, et al. Vitamin A and D intake in pregnancy, infant supplementation and asthma development: the Norwegian Mother and Child Cohort. Am J Clin Nutr 2018:107:789-798 QUESTIONS: 1. State one hypothesis the author's proposed in the manuscript. 2. There is previous research that shows that adequate Vitamin A intake is required...