Please help on part 2 not part 3. Please write in the proper reagents 112Part 2. Provide the appropriate reagents for each step in the given synthetic transformation. (3pts/box; 6 total pts)20CH₂coclA(24)Zn(19)Reduction ofmeCePart 3. Place the best answer to each question on the scantron sheet, starting with #1. (2 pts ea30 total pts)(1)ChoiceH₂C C CH₂(a) Xis a conjugated alkadiene.(b)(c)(d)

Step 1: friedel craft acylation Step 2: clemmensen reduction These two steps are explained below

Answered: 112 Part 2. Provide the appropriate…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter14: Elimination

Section: Chapter Questions

Problem 18E

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Three reactions between a Grignard reagent and a carbonyl compound are given. Draw the main organic product for each reaction and indicate if H+ or H¯ is needed to complete each reaction. The starting material structures are provided in the answer fields as a starting point for your drawings. The first reaction involves a ketone. 1. CH₂MgBr 2. H+ or H™? Select Draw / |||||| C Rings O More Erase
Draw the major organic substitution product(s) for (2R,3S)-2-bromo-3-methylpentane reacting with the given nucleophile. İndicate the stereochemistry, including H's, at each stereogenic center. Omit any byproducts. Н Br CH3CH2O (conc.)
Which set of reagents is necessary to carry out the following conversion? CH3CH₂CH₂CHCH3 O Br 1. NaBH: 2. MeOH CH₂CH₂CH₂CH₂CH₂OH O 1. (CH)3COK; 2. BH3-THF: 3. H₂O2/NaOH/H₂O O 1. H30: 2. H₂O O 1. (CH)30H: 2.BH3-THF: 3. H₂O2/NaOH/H₂O O 1. (CH) 3OH: 2. H₂O₂/NaOH/H₂O
Gg.201.
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.
1. NaBH4 2. EtOH 1. excess CH3MgBr 2. H2O 1. excess DIBAH 2. H2O 1. (CH3) 2CuLi 2. H2O
Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Supply the reagent for the reaction shown below.
Provide an arrow pushing mechanism for the following transformation. Draw out a representation of the transition-state in the rate-determining step.
In each reaction box, place the best reagent and conditions from the list below.
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Synthesize the following compound from cyclohexanol using any other organic or inorganic compounds. HO. Part 1 out of 2 Preparation of the Grignard reagent: Book rint rences OH draw structure ... draw structure... Draw the intermediate product formed above and select the correct reagent A. O MgBr, O CH;Br O Brz PB13 Draw the intermediate product formed above and select the correct reagent B. O MgBr O Mgo O O Mgl, O Mg Hint Prev 3 of .8 Next > re to search
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