II. Predict the products of the ff: elimination reactions and show the mechanisms involv HO H2SO4 (a) (b) CH3CO2N CH3CO,H (c) CH3 OH H2SO4 -CH3
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![II. Predict the products of the ff: elimination reactions and show the mechanisms involve.
HO
H2SO4
(a)
(b)
CH3CO2N
CH3CO,H
(c)
CH3
OH
H2SO4
-CH3
H](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F5bdd1e13-ff3c-4e28-ab7c-41506e6ba8f3%2Fdb4141e7-8157-4f0d-ab3e-dddce6986f93%2Fge3jzgs_processed.jpeg&w=3840&q=75)
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- 4 Which of the following alcohols could not be made selectively by hydroboration-oxidation of an alkene? Explain. about the (b) (a) (c) OH | CH3CH₂CH₂CHCH3 In H OH (CH3)2CHC(CH3)2 (d) CH3 vino zbiory 1 OH o no atou OH vollot edt evig H noituloa siblos V H но но CHO SHO=3₂HƆ m² CH3s 10 out of ST bewollot giaylonoso no WBTⱭ 12-8 His to edustrie 5 wode, $2-8 OnMX dilw osviel vitabII. Predict the products of the ff: elimination reactions and show the mechanisms involve. (a) HO H2SO4 (b) CI CH3CO2N. CH3CO2H (c) CH3 HO- H2SO4 CH3Provide the products for the reactions shown below. Suggest a reasonable mechanism (show electron flow or provide a brief explanation) to account for each step, paying attention to stereochemical details. (a) OBn 1. EtO)2CO, NaOEt 2. H* 3. H₂O*, heat 1. NaH, THF 2. Br, THF
- 9. Plan syntheses of the following compounds. You may use the given starting material and any compound containing three or fewer carbons. (a) OH (b) Br Br- (c) ✓ -OTS (d) OH(c) Write a mechanism to account for the products of the following reactions: CH3 CH, H3C. H3C. -H,0 OH -CH3 H,SO, H;C CH3Chemistry 3. Provide reagents/conditions to accomplish the following syntheses. Several steps are required in some cases. (c) (d) H2N. NH2 но H. NH2 но
- Predict the product(s) for each reaction below. In each case, draw the resonance forms of the intermediate to explain the observed regiochemistry. (a) (b) (c) (d) CN CH30. CH3 HNO3 H₂SO4 CH₂ (CH₂CHCI, AIC? Cl₂, FeCl3 ? B. CUCS.10. Describe the product formed as a result of the reaction between cyclohexanone and 3-butene-2-one by also writing the mechanism of the reaction. 1'CH,ON H;C, 2 HO CH,ep by step using arrows pushing) mechanisms that account fo the products of the following reaction (a) H₂N. Br H₂O HO H IN N.
- Predict the major products of the following reactions, including stereochemistry where appropriate. (a) cyclooctanol + NaOCl/HOAc (b) cyclopentylmethanol + CrO3 . pyridine . HCl* Predict the products and stereochemistry for the following reduction reaction NaBH4 (a) EtOH H2 Lindlar catalyst (b) 3-Hexyne (c) 3-Hexyne (d) CEC H2 Ni₂B (P-2) Na NH3Provide the structure(s) of the expected major organic product of the reaction shown. 1) Disiamylborane 2) H₂O₂, NaOH OI O II ||| O IV OV CH3CH₂C(CH3)2C=CH OH OH xx xo IV
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