Please EnCircle or Fill-In your Choice CLEARLY:21. Please Sketch the intermediates for each step below.Draw the Product which would result from the following series of reactions.Name each Type of Rx:1. Br2, FeBr32. Mg, ether3. ethylene oxide4. H₂O+5. PBr36. Mg, ether7.8. H3O+, heat (-H₂O9. HF?

Step-by-Step Reaction Analysis:Br2, FeBr3 (Electrophilic Aromatic Substitution -…

Answered: Please EnCircle or Fill-In your Choice…

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter10: Alcohols

Section: Chapter Questions

Problem 10.50P

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Solve last two questions with explanation please
Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps enter "none" for step 3. Alcohol Starting Materials Reagents Available 1. methanol a. LIAIH4 f. PBr3 k. CH3CH,CH,MgBr 2. ethanol I. CgH5MgBr (phenylmagnesium bromide) b. H2SO4 g. CrO3 3. 1-propanol с. НС h. NaH m. (CH3)2CHMgBr 4. 2-propanol d. HBr i. CH;MgBr n. pyridinium chlorochromate (PCC) 5. cyclohexanol e. SOCI2 j. CH3CH2M9B Write the number/letters of the alchol/reagents in the boxes below. Alcohol starting material Reagent for step 1 Reagent for step 2 Reagent for step 3
Provide the major organic product for the 1. LilH 4 2.нсін, о Provide the major organic product of the following reaction. following reaction. ?. 6. Provide the major organic product for the following reaction. HO Br OH NH - Br 1. LIAIH4 2. HC1, H₂O 7. Provide the major organic product of the following reaction. concentrated KMnO4 reflux
2. Cyclic esters are usually called lactones. They also undergo double Grignard additions leading to ring opening. Provide the product and a step-by-step mechanism for this reaction. 1. CH3MgBr (excess) 2. H3O+
Please rpedict the product of the given reaction - please be as detailed as possible in your explanation.
The oxidation of alcohol functional groups provides for a new electrophilic center that can be used in synthesis. Consider this two-step reaction involving an oxidation and a nucleophilic attack and answer the questions that follow.
11. Provide the major organic product of the reaction shown below. I. LIAIH, 2 H,0 co,H 12. Provide the major organic product of the following reaction. -NH2 acetic anhydride 13. Provide the major organic product of the following reaction. CO,H SOCI, 14. Provide the major organic product of the following reaction. OH conc. KMNO4, heat
Which solvent would be used for a reaction using a Grignard reagent (RMgX)?
Write the product or products that will be formed as a result of the reactions given below.
Fill in the missing structure(s) for the reaction pathways shown below. Provide allstarting material(s), reagent(s), or product(s). If more than one product can be formed,draw all major products. If more than one starting material or reagent is possible, writeall starting materials and reagents.
Write the number/letters of the alchol/reagents in the boxes below. Alcohol starting material Reagent for step 1 Reagent for step 2 Reagent for step 3
b. An alkyl halide, CsH₁1Br undergoes hydrolysis to form a 3° alcohol, CsH12O. i. ii. Br x H₂O OH SEP Provide the correct IUPAC name of the alkyl halide. State and propose the complete mechanism for the conversion of the alkyl halide to alcohol. Use curved arrows notation.

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