1. (10 points). Draw a stepwise detailed mechanism for the following reactionshowing all the substitution and the elimination products formed. Label thetype of the mechanism (SN1, SN2, E1 or E2). Show stereochemistry whenapplicable.BrCH3CH2OHH₂O2. (10 points)0BrCH3O NaDMSODraw the detailed mechanismshowing ALL possible productsformed including stereochemistryand Label mechanism as SN1,SN2, E1 or E2. Showstereochemistry when applicable.

If you have any confusion related to any step of mechanism, you can ask!

Answered: 1. (10 points). Draw a stepwise…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 45E

See similar textbooks

Similar questions

Determine the mechanism of nucleophilic substitution of each reaction and draw the products, including stereochemistr CH₂CH3 CI Br + CN d. + CH3COOH a. acetone + -OCH3 e. DMF f. b. C. ||||| a ||||| Br H Br CH2CH2CH3 + CH3OH DMSO H CH3 CI Br + OCH₂CH3 + CH3CH₂OH
H3C a. (6 points) Provide the curved-arrow mechanism for the first halogenation reaction; reaction intermediates are provided. H H e.. : OH Na H₂C H :|-| H3C
2. a. b. d. C. oFor each reaction, draw the product(s) and circle the mechanism(s). Include "major be and “minor" when necessary. Stereochemistry must be included for stereoselective reaction "No reaction" is a possible answer. Br Br ts Br CI ta ха но Br CH3ONa CH₂OH KSH acetone Br₂ hv CH3OH NaCN DMSO ser nongaholds zid) no baard E2 E1 SN1 SN2 X. E2 E1 SN1 SN2 X. E2 E1 SN1 SN2 X. E2 E1 SN1 SN2 X• E2 E1 SN1 SN2 X• E2 E1 SN1 SN2 X.
The reaction shown can give two different mono-alkylation products depending on the conditions. Draw the kinetic and thermodynamic products of the reaction. 1. base Kinetic + Thermodynamic Products 2. CH3CH₂Br (1 equiv.) Draw the kinetic product. Draw the thermodynamic product. Select Draw Rings More Erase Select Draw Rings More Erase / ||| ||| C H O / || III C H O
Draw the major organic product for each of the hydroboration-oxidation reactions. Disregard stereochemistry. Draw the product of Reaction A. Select Draw Rings More ||||||CH|OB Reaction A. 1. B₂H6 2. H₂O₂ (aq) 3M NaOH Reaction B. 1. B₂H6 2. H₂O₂ (aq) 3M NaOH S 3 Draw the product in reaction B. Select Draw Rings More |||||||||CH|OB Erase Q2Q Erase Q2Q
choice. b. (4 pts) Assign configurations ( R or S ) to all stereocenters in the products. vs. (1 pt) Unlike NaBH4, reductions carried out with DIBAL require quantities equimolarof DIBAL and substrate. Can you explain this difference? MinOR Help wirh part B please, please show working out
Joe chemist tried to make cyclopentadienone by performing an E2 elimination reaction on 2. The product that he isolated did not contain bromine and it had a molecular formula of C10H&C 7. Br a) Draw the isolated reaction product (C10H8O2) Base rg... ati... 10... b) briefly explain how this product is formed in two sequential reactions
79 3. Complete the following reaction and write a mechanism for both the substitution and elimination products (both substitution and elimination products occur simultaneously). Discuss all criteria including stereochemistry when a chiral secondary primary alkyl halide with (S) configuration reacts with methanol a weak nucleophile. Draw energy profile for this reaction. (4 points) CH2CH3 CH₂O-Na+ + Br H3C (S) no 1999b 02.907 90 +20110
give transformation
Draw the main products B-C of each of the following reactions
Can I get help with this?? Im lost, ignore my work
show mechanisma and products .

SEE MORE QUESTIONS

Recommended textbooks for you

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS