Give the major organic product(s) for each of the following reactions. Write NR if a reaction will not occur ### Organic Chemistry Reaction Schemes and Products#### (h) Reaction Scheme:**Starting Material:**- Cyclohexyl methanol (represented as a six-membered cyclohexane ring with a hydroxymethyl group).**Reagents and Conditions:**1. **MnO₂:** Oxidation step converting alcohol to an aldehyde. - **Product A:** Cyclohexanecarboxaldehyde.2. **NaCN, HCl:** Nucleophilic addition leading to the formation of a cyanohydrin. - **Product B:** 2-Cyclohexylacetonitrile (addition of a CN group).3. **HCl, H₂O:** Hydrolysis of the nitrile to a carboxylic acid. - **Product C:** Cyclohexaneacetic acid.#### (i) Reaction Scheme:**Starting Material:**- 1-Hexyne (linear six-carbon alkyne).**Reagents and Conditions:**1. **BH₃/THF followed by H₂O₂, OH⁻, H₂O:** Hydroboration-oxidation process converting alkyne to aldehyde or ketone. - **Product A:** 1-Hexanal (conversion to an aldehyde).2. **CH₃MgBr followed by H₂O or H₃O⁺:** Grignard reaction forming a new alcohol. - **Product B:** 2-Methylheptan-2-ol (addition of the CH₃ group).#### (j) Reaction Scheme:**Starting Material:**- Benzene.**Reagents and Conditions:**1. **AlCl₃, Acyl Chloride (Cl-C(═O)-CH₃):** Friedel-Crafts acylation. - **Product A:** Acetophenone (addition of acyl group).2. **Triphenylphosphine, Alkene Formation:** Wittig reaction for alkene formation. - **Product B:** Formation of a carbon-phosphorus double bond complex leading to an alkene.Each section above outlines the starting materials, reagents used, and the expected products of the reactions, adhering to common organic chemistry reaction types such as oxidation, hydroboration-oxidation, Grignard addition, and Friedel-Crafts acylation.

Answered: Image /qna-images/answer/275d5d5e-1d6b-4b23-9d46-4690a4e09cbc.jpg

Answered: MnO2 NaCN HCI HCI B H20 h) C (Give all…

MnO2 NaCN HCI HCI B H20 h) C (Give all products 1. CH3MGB. A 2. H20 or H3O* 1. ВН+/THF i) E 2. H2O2, OH", H20 Give all 2 products

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

Give the major organic product for the following reaction
Provide the starting organic reagents to prepare each of the following products using the specific reaction type if it is indicated. b. Baeyer-Villiger
Provide the curved-arrow mechanism to account for the following electrophilic aromatic substitution reaction. .CI Cl2 FeCl3
Draw the structure(s) of the major organic product(s) of the following reactions.
[Reference Draw a structural formula for the major organic product of the reaction shown below. C(CH3)3 + CH₂ (2) a H3C 2 • You do not have to consider stereochemistry. CuLi ether H₂O +
What type of alkene is Compound X? (Use all reaction information to solve for Compound X's structure.)
1) Complete the following reaction and provide a detailed, step-by-step mechanism for the process. HBr
Please provide a complete, detailed curved-arrow mechanism for the following reaction.Include ALL lone pairs and formal charges. Using the mechanism and a few words,explain the why the NaH deprotonates at the selected a-position and not the other a-position. Also explain why the indicated alkene is formed in the 3rd step rather than the other possible alkene product.
The reaction of a phosphonium ylide with a ketone or aldehyde produces an alkene, but, as shown in Problem 17.57, the reaction of a sulfonium ylide produces an epoxide. Explain why. Hint: What is the major driving force for the Wittig reaction to produce an alkene? The S-O bond energy in dimethyl sulfoxide is 362 kJ/mol.
Question:In organic chemistry, explain the concept of stereoselectivity and provide an example reaction where stereoselectivity plays a crucial role in determining the product formation.
1. The following diagram shows the partial synthesis of an important antihistamine drug currently used in the United States. One of the carbon atoms has been marked with an asterisk (*) to make it easy to spot as it undergoes structural changes from one product to the next. (a) In the box provided beneath each structure below, NEATLY write in the oxidation state for the starred carbon (*C) within that compound. Be sure to show your work in the space provided below. (b) Circle the appropriate label below each reaction arrow to indicate whether each step is an oxidation reaction, a reduction reaction, or neither. Compound A Compound B Compound C CI CI -CI N. Step 1 Step 2 Circle one: Circle one: N. oxidation oxidation reduction reduction neither neither Oxidation state of *C Oxidation state of *C Oxidation state of *C Show your work/calculations below: Compound A: Compound B: Compound C: