Question 9 Propose a chemical structure for the name below. Make sure to clearly define the stereochemistry where applicable: (E)-3,7-dimethyl-2,6-octadien-1-ol A B C D A B OH C D OH .OH OH
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![Question 9
Propose a chemical structure for the name below. Make sure to clearly define the stereochemistry where applicable:
(E)-3,7-dimethyl-2,6-octadien-1-ol
A
B
C
D
A
B
OH
C
D
OH
.OH
OH](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F1bf72abb-7d41-4f4a-ba83-6fe570fb14d9%2Fc42b1842-16b7-4804-8bfb-1a61fbc0c1e9%2Fem9oxl5_processed.jpeg&w=3840&q=75)
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- 2. Show the mechanism with arrow formalism to show the formation of the most stable product. Which of the following terms apply to the mechanism(s) i) Regioselectivity (ii)stereoselectivity (iii)stereospecificity. Explain H+ (aq) from sulfuric acid NaCN most stable producthelp with #18Draw the structure of the expected organic product(s) formed in the following reactions including correct stereochemistry. If the product is racemic write both isomers or write racemic. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state 'No Reaction'
- Draw a structural formula for the product formed when 2,2-dimethylpropanal is reduced by hydrogen in the presence of a transition-metal catalyst. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. | 3 0. 8) ©////-000- [F CH₂ ChemDoodle Complete the following reaction by writing the name of the product. CH₂ 0 + H₂ Ni or Pt ?42 and 43Draw structural formulas for the following the compounds: (d) cis-1,3-dicyclohexylcyclopentane (e) (Z)-2-cyclohexyl-4-methylhept-2-en-3-ol (f) 3-methoxybenzaldehyde
- Do not use chatgpt. Thank you!Practice Problem 07.48g Assign a systematic (IUPAC) name for the following compound: Br 4-bromo-4-(1,1-dimethylpropyl)heptane O 4-bromo-4-(1,1-dimethylpropane)heptane 4-bromo-3,3-dimethyl-4-propylheptane O 4-bromo-4-neopentyiheptane MacBook Air9. Write structural formulas for the major organic product(s) for the following reactions. Be sure to indicate stereochemistry when relevant. (CH;CH,CH,),CuLi (a) Cl Br PAL2 (b) HO (c) CH;CH,CH,CH,OH C,H5MgBr 10. Propose a reasonable mechanism for the following reaction Be sure to include all intermediates. (transition states are not necessary) Br Br hv CH3-CH=C(CH3)2 + Br, ČH,-CH=C(CH3)2 CH2=CH–Ċ(CH3)2 11. Indicate how each of the following compounds could be prepared using the given starting material CH;CH,CH,CH3 CH;CH,CH,CH,Br CH;CH,CH,CH3 H,C=CH-CH=CH2 Br CH;CHCH,CH3 CH;CH=CCH,CH3 CH3
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