Provide the multistep synthesis for the following reaction. Include reagents:
Provide the multistep synthesis for the following reaction. Include reagents: он сн, сH, .CH CH Н.С Н, с
6. Give IUPAC names for the following compounds b) а) CH,-CH,-CH-сH-с-сн, -сн, -сн, сн, CHCH X Cн, CH,-CHCH) - CH-сH, -CH Н CH CH С-с н нн CH2 CH CH(CH) Н.С - СH-СН-СН-СH н Н н сн, сн, CH С -с CH h) CH, -CH, -сH CH3 i)
7. What redox coenzyme is most likely to be involved in the reaction below? он O LLL он он CH,-с—сн,-сH-сH,-с-он сH-сн—сн,-снсн,-с-он a. NADPH b. NADP+ c. NAD+ d. FAD e. This reaction does not require a coenzyme.
Provide the multistep synthesis for the following reaction. Include the reagnets. ОН Н Br Br
CH3 H2SO4 н,с. OH сH, 2. OTs SH NaSH н, с сH, OTs No reaction H,с. Cн, o CH3 HBr Br HO H,с CH Provide the reagents necessary to carry out the following conversions. Br SH NadH NasH
Examine the following compounds. CH3-CH2-CH2-CH)-CH2-CH3 НО-СН-СН-CH--CH--CH-ОН С A ОН Но-СН--СH-CH-CH--CH-ОН CH--CH-CH-СH--CH-ОН D would be the most soluble in water Structure O A В O C O D
2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе most stable least stable (a) I (b) I (c) I ll (d) 7) Order the following C-H bonds from strongest to weakest. strongest weakest (a) (b) (c) II (d) 8) Which of the following is represents the lowest energy transition state for the addition of BH, to 2-methyl-1-propene? quCH «сHs нСи Нас (b) (a) Нив--н H H...
Draw the Haworth projection of the image below. Сн,он 20 НО-С-н н-с-он Н-С-ОН Сн,ОН
Is this structure tetrose, pentose, hexose or triose? Сн,он с=0 — н-с-он н—с-он НО-С-н Сн,он Порно ви Динална на на Ketose
Select all the pairs that are cis-trans isomers. Н Н-с— сн, н and H;C HаС — сн Н Нс Н.с—сн, н and H. Н Нас— сн H. Нс CH3 н CH3 CH-CH CH-CH and Н Н н.с н Н,с—сн Н,с—сн, H. and CH, Н,с H. H. semsof use contact u about us privacy policy help careers F7 FS F6 F3 & 8 4 { Н G
Which of the following isn't a chiral molecule? Н.С. HC Н.С CH, CH Н;С CH СН3 B D А с