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2. Starting with ethyne and any necessary reagents to synthesize enantiomers of (3S,4R)-4-bromo-3-hexanol and (3R,4S)-4-bromo-3-hexanol. H5C2...
2. Starting with ethyne and any necessary reagents to synthesize enantiomers of (3S,4R)-4-bromo-3-hexanol and (3R,4S)-4-bromo-3-hexanol. H5C2 H5C2 H -ОН НО-Н Several steps HC-CH H -Br Br -H C2H5 C2H5
The major product of the acid-catalyzed hydration of (E)-3-methyl-3-hexene is a. (3R,4S)-4-methyl-3-hexanol exclusively b. (S)-3-methyl-3-hexanol exclusively c. 4-methyl-3-hexanol racemic mixture of two enantiomers d. (R)-3-methyl-3-hexanol exclusively e. (3S,4R)-4-methyl-3-hexanol exclusively f. 3-methyl-3-hexanol
Question 3 1 pts What is the IUPAC name for the following compound? O (3S,4R)-3-bromo-4-methylhexan-2-one O (3S,4S)-3-bromo-4-methylhexan-2-one (3R,45)-3-bromo-4-methylhexan-2-one O (3S,4R)-3-bromo-4-methylhexan-2-one 3-bromo-4-methylhexan-2-one 0 4-methyl-3-bromohexan-2-one
(2) Hta H- CH CAH CH3 is properly named: A) (3R.4S,5R)-3,5-Dichloro-4-methylhexane B) (2S,3S,4S)-2,4-Dichloro-3-methylhexane c) (2S 3R 4R)-2,4-Dichloro-3-methylhexane D) (25.3R.45)-2,4-Dichloro-3-methylhexane E) (2S,3S,4R)-2,4-Dichloro-3-methylhexane AO BO co DO Е О MacBook Air
1. Draw a structure for: (Z)-3-Bromo-2-hexene (Z)-1-methylcyclononene (3Z,6E)-1,3,6-Octatriene (E)-2-methoxy-2-pentene (3S,4S)-4-methyl-3-hexanol (1R, 3S)-3-methylcyclohexanol
Draw the structures for the following compounds. a) (3Z,5S)-4-bromo-5-chloro-2-methylhexa-1,3-diene b) (5S,7S)-5-(bromomethyl)-7-chloro-oct-2-yne c) (1S,5S,6S)-6-bromo-5-[(1R)-1-chloroethyl]cyclohex-3-enol d) 2-bromo-4-[(1R)-1-hydroxyethyl]benzoic acid e) (3S,4S,5S)-5-amino-3-hydroxy-4-methylhexanal f) (Z,2R,4R)-6-bromo-4-chloro-N-ethyl-N-methylhept-5-en-2-amine g) [(1S)-1-chloroethyl] (Z,3R)-5-chloro-3-methoxyhex-4-enoate h) (Z,3R)-3-bromo-4-chloro-7-methyloct-4-enoic acid i) (3S)-6-bromo-N-ethyl-N,3-dimethylhex-4-ynamide j) (Z,3R,4S)-6-bromo-3-[(1S)-1-chloroethyl]-4-hydroxyhept-5-en-2-one
Devise a synthesis of (Z)-3-octene using one of the starting materials and any of the reagents below using the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in the remaining unused steps Starting materials нсисынсно-си нос-сцен нос-cң соң,он нонс Reagents + NaNH / NH diodo ethane 1-bromo-3-methybutane H undar catalyst + NaOH HẠO e 1-bromopropane butyl bromide күн clodomethane 1 2-bromopropane H/Pd on carbon I N/NH0 Starting material Reagent for step 1...
CHEM 2060 HOMEWORK #4 Chp. 5 and 6 Due March 5th, 2020, 1:20 PM! 1. Fill in the squares with the corresponding chirality (R or S) for the following pairs of chemical structures and determine whether they are Enantiomers, Diastereomers or the Same Compound. (20 points total) U - Br FT NH2 NH2 Br COH A) Enantiomers COZH C) Same Molecule B) Diastereomers CH3O HSCH CICH2 FH Hс-н H CH3 CHCI SHU A) Enantiomers B) Diastereomers C) Same Molecule back...
1. Name the following compound. A. (3S,4R)-8-chloro-4-methyloctan-3-ol B. (5S,6R)-1-chloro-5-methyloctan-6-ol C. (3R,4S)-8-chloro-4-methyloctan-3-ol D. (5R6S)-1-chloro-5-methyloctan-6-0l Cl OH 2. What is the reagent needed for the following chemical transformation? OH Cl A. SOCl2, Pyr B. PBr3 C. HCI D. XeCl5
7. 3) What term describes the structural relationship between (2R, 3R, 4S) - 2, 3 trichloroheptane? - trichloroheplane and (25, 3S, 5R) - 2, 3, 5 , 6. 2) What term describes the structural relationship between cr-1.2-dimethylcyclopentaneand dimethyleyelopentane? A) not isomers B) constitutional isomers C) enantiomers D) diastereomers E) conformers 7. 3) What term describes the structural relationship between (2R 3R.45)-23 A-trichloroheptane and (25,35,5R)-2.3.5- trichloroheptane? A) not isomers N B) constitutional isomers C) enantiomers D) diastereomers _E) conformers 8. 7)...