1. Assign E or Z to the following alkenes. If the alkene does not have stereochemistry, write "NONE".HCIH3CSHT.HCI,ОНH3CH2CНОDDENC(CH3)3CH3MeHEtN''N'C=CH3CEtMewhat Columbus sought in the 'Indies' - PiperineCH2OHBr(H3C);C,H3CHOH, CH,CF,H3CBrHOH2CНОHthe spice Columbus found (Capsaicin)HO.MuscalureBombykol(the sex attaractant for the male silkworm)(the sex attaractant for the common housefly)OH.CO2Hthe "heart healthy" part of olive oila 'less healthy' trans fatty acid from trans fat

since you have posted a question with multiple subparts we are entitiled to answer only first 3…

1. Assign E or Z to the following alkenes. If the alkene does not have stereochemistry, write "NONE". H CI H3C SH H. OH H3CH2C D НО C(CH3)3 CH3 .N. H. Me Et D. Et Ме H3C what Columbus sought in the 'Indies' - Piperine Br- CH,OH (H3C);C, H3C HOH, CH,CF, H3C Br HOH2C H НО the spice Columbus found (Capsaicin) HO, Muscalure Bombykol (the sex attaractant for the male silkworm) (the sex attaractant for the common housefly) LOH .CO2H the "heart healthy" part of olive oil a 'less healthy' trans fatty acid from trans fat

1. Assign E or Z to the following alkenes. If the alkene does not have stereochemistry, write "NONE". H CI H3C SH H. OH H3CH2C D НО C(CH3)3 CH3 .N. H. Me Et D. Et Ме H3C what Columbus sought in the 'Indies' - Piperine Br- CH,OH (H3C);C, H3C HOH, CH,CF, H3C Br HOH2C H НО the spice Columbus found (Capsaicin) HO, Muscalure Bombykol (the sex attaractant for the male silkworm) (the sex attaractant for the common housefly) LOH .CO2H the "heart healthy" part of olive oil a 'less healthy' trans fatty acid from trans fat

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter8: Addition Via Carbocation

Section: Chapter Questions

Problem 3CTQ

See similar textbooks

Similar questions

The synthesis above can be performed with some combination of the reagents listed below. Give the necessary reagents in the correct order. Be sure to consider stereochemistry and regiochemistry.A. NaOHB. mCPBAC. OsO4, tBuOOHD. NaHE. H2, LindlarF. CH3CH2CH2BrG. CH3CH2ClH. NaNH2I. H3O+J. Na, NH3(l)
A chemist allows some pure (2S,3R)-3-bromo-2,3-diphenylpentane to react with a solution of sodium ethoxide(NaOCH2CH3) in ethanol. The products are two alkenes: A (cis-trans mixture) and B, a single pure isomer. Under thesame 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 structuresof A, B, and C; give equations for their formation; and explain the stereospecificity of these reactions
Is the following alkene E,Z, or neither? a. E b. Z c. neither d. It is one or the other, but which is impossible to determine from the information given
1. i.What are the various ways by which alkenes may be synthesized? ii. Give two examples each of Unsymmetrical alkenes and reagents. iii. Give two examples of reactions of alkenes that result in Anti-Markonikov’s addition products
What starting alkene reacted with I2 in a solution of CH2Cl2 is required to produce 1,2-diiodoocyclopentane?
best condition for the reaction (1r,2s)-1 bromo-2methylcyclohexane->(s)3-methylcyclohex-1ene
Show how to control the stereochemistry and regiochemistry (orientation) of additions to alkenes to obtain the products we want.
Assign the stereochemical configuration (E or Z) for the alkene below. Show your work, indicating clearly which groups are assigned high priority (e.g., through assigning the groups numbers, circling only the high priority groups, or labeling groups as high or low).
Fill in the following missing organic structures. Consider stereochemistry (R/S and/or E/Z –cis/trans) and possible carbocation rearrangements.
a. Identify two alkenes that react with HBr to form 1-bromo-1-methylcyclohexane without undergoing a carbocation rearrangement. b. Would both alkenes form the same alkyl halide if DBr were used instead of HBr? (D is an isotope of H, so D+ reacts like H+.)
OChem HELP... Draw the conformational structures (chair or boat conformations) for the MAJOR product formed when 1-tert-butylcyclohexene reacts with each of the following reagents. Also, indicate if the product obtained is racemic form. a) Br2, CCl4 b) Br2, H2O c) OsO4, then aqueous NaHSO3 d) ICl e) mCPBA, then H3O+, H20 f) O3, then Me2S (conformational structure not required) g) BH3:THF, then H2O2, HO- h) D2, Pt i) Hg(OAc)2 in THF-H2O, then NaBH4, HO- j) BD3 :THF, then CH3CO2T
What would the final products look like? (specify stereochemistry if needed)