major product of the following reaction for letter d) and explain the mechanism/process

Q: NH2

A: The given reagent is Di-tert-butyl dicarbonate which is commonly known as Boc anhydride. It is a…

Q: CN DIBAL-H, -78 °C

A: DIBAL-H is a mild reducing reagent. DIBAL-H react with nitrile formation of imine followed by…

Q: Consider the reaction scheme shown below. HCI [1] HO. (a) Provide a detailed mechanism for reaction…

A: This reaction will occur via 3 step. In first step protonation then Water molecule eliminate to…

Q: For each of the following, show the mechanism(s), write the MAJOR product(s), and, when applicable,…

A: alkyl halides participate in both elimination and substitution reactions based on reaction…

Q: The following isomers react separately with sodium hydroxide to give different products with the…

A: First isomer has close –OH with –Cl and second isomer have 2 groups at more distance to each other.

Q: b) OH OCH, d) H 1) CH3MgBr 2) H₂O* 1) SOCI₂, heat 2) (CH3CH2)2CuLi 3) H₂O 1)2 eq. CH3CH2MgBr 2) H₂O*…

A:

Q: Complete the following reaction:

A: Alkene gives hydration reactions in the presence of an acid catalyst. The reaction follows an…

Q: F H3C AICI 3 Br

A: The reaction is Friedel-Crafts alkylation of fluorobenzene involves substitution of a hydrogen atom…

Q: Provide the mechanism and product

A:

Q: LOEt NaOEt, EtOH

A: The given reactant is an ester. It has one electrophilic center as well as an acidic proton.The…

Q: Give the complete detailed mechanism for the following reaction

A: In the given reaction the acid chloride reacts with methoxide ions to form an ester, by nucleophilic…

Q: Provide the MAJOR product of the following reaction and draw the curved-arrow

A: Regiochemistry is the chemistry of regioselective reactions Regioselectivity is the priority of…

Q: (b) How can be prepared from OEt CO,Et and at EtO OEt EtO2C 95 °C ? Provide the mechanism.

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Q: Starting from benzene, synthesize the following compounds. Write the complete reagent/s and…

A:

Q: Give the major organic product of the following reaction for letter e) and explain the…

A: When the alpha, beta-unsaturated carbonyl compound is treated with the Grignard reagent it undergoes…

Q: 10. Use the step-wise mechanism to predict the product of the following Friedel-Crafts Acylation…

A: Friedel-Craft acylation reaction:Benzene gives an aromatic electrophilic substitution reaction. The…

Q: H* 2. H2O

A: Alkene mainly gives electrophilic addition reaction in which an electrophile attacks on electron…

Q: (a) Identify the major product of the following reaction. (b) Explain why the other product is not…

A: a) The major product is (II). b) The reaction is followed the mechanism of Friedel-Crafts…

Q: но ногом 0 Н. ен Н. за у (osnx7) Н -он

A:

Q: H H A CI AICI; Br I. I'

A:

Q: For each reaction, draw the complete mechanism and the major organic product. (a) (b) excess HCI ?…

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Q: H20, H2SO4 -OH-

A:

Q: NaCN NH3 NaN3 NH reagents/solvents of your choosing ?

A: This question is from basic reaction mechanism.

Q: 3c）Referring to the intermediates you drew in problem below explain in detail why no meta product is…

A:

Q: 10. 9. Br HOC HOC Meo Br 1. Con 12. OH OH 13 14. Br Br Br Br

A: There are several reactions mentioned here involving the participation of aromatic, carbonyl and…

Q: Provide the mechanism 9. 3%aq-HGH major Minor LDA. IHF KOBut ELOH OH $% NoOH HO Ha keto tautomer

A:

Q: (a) Determine all possible products from the following reaction. Also, identify the products as…

A: (a) Given reaction,

Q: 1. Provide the mechanism for the following reaction. N=N BNO BnO ...OCH3 ...OCH3 PPh BzO OBN HO OBN…

A: This reaction is Known as mitsunobu reaction in which there occurs change of stereocentre.

Q: Provide the major organic product of the reaction below. HBr

A:

Q: Н О день - Воно + (ii) (!) (iii) Н НО + H2O HOO > НО H он + Oʻн + OH2 НО + НО_ H300

A: Since it is a multiple question I am solving first question only as per the answeringguidelines.…

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.