1
answer
0
watching
213
views
11 Nov 2019
Problem 4. Refer to the reaction below and circle the correct answers. 2 pts each cata a commerical fragrance a. Classify b. Identify the above mechanism as polar, radical, orpericycli c. How many transition states occur in the above reaction? 1, 2/3 or 4? d. How many intermediates are formed in the above reaction? @a or 4? e. True or false? Enantiomers could be formed based on the information provided. the above reaction as an addition, elimination, substitution. rearrangement Problem 5. Draw the two chair conformations of cis-1,2-dimethylcyclohexane as Newman projections looking down the Ct-C2 and Cs-Cs bonds. Clearly label which is the most and which is the least stable conformation. If they are of equal stability, you must clearly state so. 6 pts eaval stablHy Problem 6. Draw the two chair conformations of trans-1-(tert-bu trans-1-(1,1-dimethylethyl)-3-methylcyclohexane), and identify each substituent as either axial or equatorial. Clearly label which is the most and which is the least stable conformation. If they are of equal stability, you must clearly state so. 6 pts ty)-3-methylcyclohexane (i.e. arial axãa avto Most stable least stable
Problem 4. Refer to the reaction below and circle the correct answers. 2 pts each cata a commerical fragrance a. Classify b. Identify the above mechanism as polar, radical, orpericycli c. How many transition states occur in the above reaction? 1, 2/3 or 4? d. How many intermediates are formed in the above reaction? @a or 4? e. True or false? Enantiomers could be formed based on the information provided. the above reaction as an addition, elimination, substitution. rearrangement Problem 5. Draw the two chair conformations of cis-1,2-dimethylcyclohexane as Newman projections looking down the Ct-C2 and Cs-Cs bonds. Clearly label which is the most and which is the least stable conformation. If they are of equal stability, you must clearly state so. 6 pts eaval stablHy Problem 6. Draw the two chair conformations of trans-1-(tert-bu trans-1-(1,1-dimethylethyl)-3-methylcyclohexane), and identify each substituent as either axial or equatorial. Clearly label which is the most and which is the least stable conformation. If they are of equal stability, you must clearly state so. 6 pts ty)-3-methylcyclohexane (i.e. arial axãa avto Most stable least stable
Reid WolffLv2
9 Mar 2019