**Learning Target 16****Criteria for Satisfactory Score:**- Reactants, products, and reagents that complete a reaction scheme must specify compounds, not generic categories.- Reagents and structures must be valid Lewis structures.**Tasks:**- Complete the synthetic sequences by drawing products/substrates/reagents in empty spaces in reactions below.**Reaction Sequences:**1. **Reaction 1:** - Starting compound: - An alcohol with a branched chain, depicted as HO-. - Reagents: - 1. PBr₃ - 2. Mg, dry ether - 3. CH₃CH₂C(O)CH₃ - 4. H₃O⁺ (acid work-up) - [Arrow indicating reaction progress]2. **Reaction 2:** - Starting compound: - Phenol derivative with OH group on a benzene ring. - Reagents: - 1. MsCl, pyridine - 2. CH₃CH₂SH, acetone - [Arrow indicating reaction progress]3. **Reaction 3:** - Starting compound: - A ketone with a benzene ring. - Reagents: - 1. LiAlH₄ - 2. H₃O⁺ - 3. conc. H₂SO₄, heat - [Arrow indicating reaction progress]4. **Reaction 4:** - Reaction of a cyclic alkene: - Reagent: diluted H₂SO₄ - Products: - Two cyclic alcohols, both with OH groups in racemic forms (a mixture of stereoisomers).5. **Figure 14: Reactions:** - Transformation of a cyclohexene derivative into a diol. - Starting compound: - A cyclohexene structure. - Final product: - Cyclohexane with two OH groups in a racemic mixture.This educational content outlines specific organic chemistry reactions, focusing on completing reaction schemes using concrete compounds and valid Lewis structures.

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Learning Target 16 Criteria for satisfactory score Reactants, products, and reagents that complete a reaction scheme must specific compounds, not generic categories. Reagents and structures must be valid Lewis structures. Tasks Complete the synthetic sequences by drawing products/substrates/reagents in empty spaces in reactions below. 1. PBr3 2. Mg, dry ether 3. CH3CH2C(O)CH3 4. H3O* (acid work-up) 1. MSCI, pyridine 2. CH3CH2SH, acetone OH 1. LIAIH4 2. H3O* 3. conc. H2SO4, heat diluted H2SO4 "OH- OH HO" HO OH racemic mixture Figure 14: Reactions

Learning Target 16 Criteria for satisfactory score Reactants, products, and reagents that complete a reaction scheme must specific compounds, not generic categories. Reagents and structures must be valid Lewis structures. Tasks Complete the synthetic sequences by drawing products/substrates/reagents in empty spaces in reactions below. 1. PBr3 2. Mg, dry ether 3. CH3CH2C(O)CH3 4. H3O* (acid work-up) 1. MSCI, pyridine 2. CH3CH2SH, acetone OH 1. LIAIH4 2. H3O* 3. conc. H2SO4, heat diluted H2SO4 "OH- OH HO" HO OH racemic mixture Figure 14: Reactions

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Ga. Carbocat AutoSave Insert 3 OFF A- V Font Draw Design Paragraph 60 12 173 words 1-methylc b. (See section 10.4) Layout A Styles Dictate Focus OH 16- Br₂ The par HBr light Tell me ChemDraw Practice 3. Double click on each of the reactions - because these were made in ChemDraw and this is a Word document, this action should take you directly to a ChemDraw. document (unfortunately, that doesn't work in a .pdf document). Generate the structure of the major product, and then close the ChemDraw, file. The partial reaction should now be replaced with the full reaction, including the final product. a. (See section 5.7) Chapter Summary... Sensitivity II Cheyy independent experiment Sally wanted = 4 Comments Editor (continued on next page) + Share 100% Show F
Solve as soon as possible please. Can you explain these two questions?
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part 2 [References] Draw the final organic product of this series of reactions. 1. CH;CH2COCI, AICI3 2. Br2, CH3CO2H 3. K* tBuo 4. OsO, then NaHSO3 5. H2Cro4 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • Do not draw organic or inorganic by-products. C P. opy aste
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Determine the best starting materials for the following reactions. J Kloster.. 2 ©2022 . CHEM40B W22 ©2022loster 122 J Klosterman CHEM40 V22 2024 V22 ©2022 J Klostermarr CHEM40B W22 ©202 RoORosterman CHEM4 22I Klogerman CHEM40B W22 2022 | K a) Klosternia CHEMOR N22 ©2 Br Prod#891502 b) I Klosten CHEM408 W22 CHEL Prod#502658 H2 H Et I Klos Et EMe Me Pd/C Write your answer in the Answer sheet template. 2022 Prod#658891
Which 2-step process would convert the reactant to the product? Excess reagent is implied if needed. Hint: Attempt this question towards the end of the exam, so flag it if you get it in the beginning. HO. Br 1. dilute sulfuric acid Br2 HBr / ROOR t-BUOK HBr conc. sulfuric acid 1) BH3-THF 2) H2O2 / NaOH TSCI, py NaOEt 2.
synthesis have flaws. explain why this is wrong and make a synthesis compound A from benzene . show solution
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Suppose you are given the starting molecule shown below. For each of the cases listed below, list the reaction conditions and reagents that would give that product, and give a brief explanation of why ONLY the specified product would be formed under the conditions you chose. Make product alcohol with OH group at carbon 1. Make product alcohol with OH group at carbon 2. Make product alcohol with OH group at carbon 3. а. b. 3 2 C.
Chapter 2 Alkylation Reaction 1. Write the main products of the synthesis reaction according to the specified raw materials, reagents and reaction conditions он H,PO, / BF3 - OE (1) Br CH,LI ether (2) CH,Br RNH2 (3) ElNMeOH Co,CH, OCH3 OMs :O Ph- H,NNH, • H0 EIOH, 60°C DMF (4) HN. DABCO, DME (5) NH2 OMe O Me,NH, MEOH (6) Meo r.t. NO Ph(CH2),Br (7) K,CO, DMF MeO THE (8) PHCH,CH,MgBr + N-CHO OAC (9) Me" 1) CH,,OK* 2) CgH,OH SnCl, 0°C (10) OMe Br
Criteria for satisfactory score Reactants, products, and reagents that complete a reaction scheme must specific compounds, not generic categories. Reagents and structures must be valid Lewis structures. Tasks Complete the synthetic sequences by drawing products/substrates/reagents in empty spaces in reactions below. 1. t-BUOK, heat 2. Br2 (1 equiv) methanol (solvent) Br 1. O3 2. Me2S 1. Hg(OAc)2, H2O 2. NABH4