### Reaction Completion and Product IdentificationPlease complete the reactions below. For reaction "b," add a substrate. For the other reactions, write down the major product(s).**Hints:** For "e," hydride from LiAlH₄ serves as the nucleophile in the first step.#### Reaction Details**a.**- **Starting Material:** Cyclohexanol- **Reagent/Conditions:** H₂SO₄, 180°C- **Expected Reaction:** Dehydration to form cyclohexene.**b.**- **Starting Material:** Phenyl lithium- **Reagents:** 1. Lithium reagent 2. H₃O⁺- **Expected Process:** Nucleophilic addition followed by protonation.**c.**- **Starting Material:** Sodium phenoxide- **Reagent:** CH₃Br- **Expected Reaction:** Williamson ether synthesis to form anisole (methoxybenzene).**d.**- **Starting Material:** 3,3-Dimethyl-1-butanol- **Reagent:** HBr- **Expected Reaction:** Conversion to alkyl bromide through substitution.**e.**- **Starting Material:** Cyclopentanone- **Reagents:** 1. LiAlH₄, (CH₃CH₂)₂O 2. H₃O⁺, H₂O- **Expected Reaction:** Reduction to form cyclopentanol.Note: The reactions detailed above are fundamental transformations often encountered in organic chemistry, with specific emphasis on mechanisms like dehydration, nucleophilic addition, Williamsons' ether synthesis, and reductions involving hydrides.

Alcohols when heated in the presence of H2SO4 give alkene Aryllithium when treated with epoxide give…

Please complete the reactions below. For b, add a substrate. For the other reactions, write down the major product (s). Hints: for e, hydride (from LIAIH4) serves as the nucleophile in the first step. a. H,SO̟ 180ºC b. 1) но. "Li 2) H¿O* LO Na+ CH,Br

Please complete the reactions below. For b, add a substrate. For the other reactions, write down the major product (s). Hints: for e, hydride (from LIAIH4) serves as the nucleophile in the first step. a. H,SO̟ 180ºC b. 1) но. "Li 2) H¿O* LO Na+ CH,Br

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...

See similar textbooks

Similar questions

The answer to this question is D, can you please draw the mechanism to get that product? 1. -MgBr H;0* workup ? OTMS 2. TBAF 3. POCI, / pyridine (еxcess) 4. Нeat он A B он CI CI D
29a. Solve for the problem in the picture
Explain why each of the following reactions will not proceed as written. [1] LDA + Co2 a. C. [2] CH;CH2I COOH [1] NaOEt b. CH2(CO,Et)2 (CH,CH2),CCH(CO̟Et)2 (2] (CH3CH2),CBr
1. Draw the major Products & 2. Et O 8 1. Ht, Br 2. Pyriding 3. Et, Culi DEE 1. NOEL /EtOH 2. велгул 3.430 + / heat 12 t2NH, CHI 2. 3. H 30+ / heat iodide for the reactions
7. The reactions shown below will NOT occur as written, Explain why (briefly), and suggest a Tix (1.e. something you could change to get the transformation to occur). a) CrOa, H* OH OH b) 1. BrMgPh Ph 2. H* но HO c) CH30 OCH3 CH3CN HO. OH d) H*, H20 오
2. Complete the reaction mechanisms started above by drawing the curved arrow for the second step of the process here-the nucleophilic attack of the halogen to the electrophilic carbocation. a. b. а d. + + Bre 1 Br -at Br Br Cl +
D. Provide a reasonable mechanism for the following reaction. -CC13 1. NaOH, H₂O 2.H₂O* ooi OH
From the reaction conditions provided, design a four-step reaction sequence that is expected to convert the starting material into the product shown? For each step, only the major expected product can be taken forward. Assume standard workup as necessary. of 1. Cros, pyridine 2. BHs, THF, H2O2, H20 3. HBr 4. (COC2)2. MeOH 5. HBr, ROOR, heat 6. NBS, light 7. tBuONa, tBuOH 8. H2SO4, H2O Step 1: choose your answer. Step 2: choose your answer. v Step 3: choose your answer. Step 4: >