What is the name of the following structure?хубаBr(3E,6Z)-7-bromo-4-fluoro-2,3,5-trimethyl-3,6-nonadiene(3Z,6Z)-7-bromo-4-fluoro-2,3,6-trimethyl-3,5-nonadiene(3E,6E)-7-bromo-4-fluoro-2,3,6-trimethyl-3,6-nonadiene(3Z,6E)-7-bromo-4-fluoro-2,3,6-trimethyl-3,5-nonadieneO (3Z,6E)-7-bromo-4-fluoro-2,3,6-trimethyl-3,6-nonadiene

Steps to follow:Step 1: Identify longest carbon chain with most substituents. Select the carbon…

Answered: What is the name of the following…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter5: Stereochemistry At Tetrahedral Centers

Section5.SE: Something Extra

Problem 70AP

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Name the following compound: Br O (1S, 3S,4R)-1-chloro-3-bromo-4-isopropylcyclohexane O (1R, 2R, 5R)-1-bromo-2-isopropyl-5-chlorocyclohexane O (1R, 2S, 4R)-2-bromo-4-chloro-1-isopropylcyclohexane O (1S, 25, 4R)-2-bromo-4-chloro-1-isopropylcyclohexane O (15, 25, 5R)-1-bromo-2-isopropyl-5-chlorocyclohexane
Draw the structures and label the priority and E,Z
Assign a systematic (IUPAC) name for the following compound: (Z)-3,3,4,5-tetramethyl-4-heptene (E)-3,3,4,5-tetramethyl-4-heptene (E)-3,4,5,5-tetramethyl-3-heptene O (Z)-3,4,5,5-tetramethyl-3-heptene
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From : cis (1s, 4s) -1-bromo- (tert-butyl) cyclohexane trans (1r, 4r)- 1- iodo- 4- isoproppylcyclohexane 1,5 - dimethylcyclohex -1 -ene trans (1r, 4r)- (tert - butyl) - 4- fluorocyclohexane trans (1r, 4r) - 1- bromo - 4- (tert - butyl) cyclohexane 1,3,5 - trimethylcyclohex - 1- ene . 5- Choose the substrate from the ones that drawn and illustrate an example complete Markovnikov addition mechanism using the reagents of your choice showing all stereochemical consequences. Identify if your addition mechanism is syn addition or anti addiction (Use curved arrows to show the electron movement in everyday steps). use ChemDraw if possible..
Please show me how you get the Name
Treating cyclohexene with Br₂ yields trans-1,2-dibromocyclohexane. Justify why the cis isomer is not formed. Br Br2 Br
Draw the compunds below. (2e,4z)-1-bromo-4-methylhexa-2,4-diene (2e,4z)-5-bromo-3-methylhexa-2,4-diene (2z,4e)-1-bromo-4-methylhexa-2,4-diene (2z,4e)-1-bromo-3-methylhexa-2,4-diene
Name (including E/Z stereochemistry) the five alkenes that can produce 3-bromo-3-methylhexane on reaction with HBr. Draw the skeletal structure of each molecule.
cis-1-Bromo-4-tert-butylcyclohexane and trans-1-bromo-4-tert-butylcyclohexane both react with sodium ethoxide in ethanol to form 4-tert-butylcyclohexene. Explain why the cis isomer reacts much more rapidly than the trans isomer.
Cyclobutane reacts with bromine to give bromocyclobutane, but bicyclobutane reacts with bromine to give 1,3-dibromocyclobutane. Account for the differences between the reactions of these two compounds. heat + Br2 -Br + HBr Cyclobutane Bromocyclobutane heat Br2 Br Br Bicyclobutane 1,3-Dibromocyclobutane
A chemist allows some pure (2S,3R)-3-bromo-2,3-diphenylpentane to react with a solution of sodium ethoxide(NaOCH2 CH3) in ethanol. The products are two alkenes: A (cis-trans mixture) and B, a single pure isomer. Under the same conditions, the reaction of (2S,3S)-3-bromo-2,3-diphenylpentane gives two alkenes, A (cis-trans mixture) and C. Upon catalytic hydrogenation, all three of these alkenes (A, B, and C) give 2,3-diphenylpentane. Determine the structures of A, B, and C; give equations for their formation; and explain the stereospecificity of these reactions.

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