(CH3CH2)2NH, mild acid NABH3CN NaOH, H2O NaOH, H20, heat

Q: H3CSH

A:

Q: NaHSO3 NaOH + CO2 OH OH OH

A: The reaction given is,

Q: OMe HO 1. LIN(iso-propyl)2 OMe 2. H20

A:

Q: NABH4 МеОн of (CH3CH2)2NH, mild acid NaBH3CN H3CSH

A: The product of the reaction is given as follows

Q: In a retrosynthetic fashion, dissect the following molecule into two parts: indicated reagents. The…

A:

Q: Propose a detailed, electron-pushing mechanism for the oxidation of the given secondary hydroxyl.…

A: Given reaction is Dess Martin oxidation.

Q: Br2 ОН Br

A:

Q: /A) Suggest a mechanism and give name for each the following reactions: ) acetic anhydride +…

A: To write : Mechanism of the following reaction          Acetic anhydride + benzaldehyde →Cinnamic…

Q: 4. Provide a arrow pushing mechanism for the following transformation. H3O+ Br2

A:

Q: Identify A, B, and C, intermediates in the synthesis of the five-membered ring called an…

A: The A,B and C cpmpounds are as given below:

Q: a OH CH2CNHCH3 CH3 C d OH CHCHNHCH3 CH3 Ephedrine can be synthesized via reductive amination plus…

A: Here we have to predict necessary reactants and reagents that will give the intermediate and final…

Q: Diazotization of aniline first involves the formation of NO* (nitrosonium ion) by the dehydration of…

A: Given

Q: D. What is the product of acid hydrolysis of the following ester with HCI CH,-CHC-O-CH-CH 1-CH3 a.…

A:

Q: ...Br t-BUOH

A:

Q: is a valuable synthetic intermediate because each of its Epichlorohydrin three carbons contains a…

A: Allyl chloride can be prepared from propene by the free radical mechanism as shown in the next step.

Q: . Propose an electron arrow pushing mechanism for the following reaction. H,SO4 SO,H

A: An electron arrow pushing mechanism for the given reaction can be shown below

Q: CH3 H₂C. Br2 CH3 FeBr3 H₂C CH₂ the bromination reaction, the bromine substituent in the product will…

A:

Q: CH2COOH CH2Br `CH3 CH3

A:

Q: Mustard gas, Cl¬CH2CH2¬S¬CH2CH2¬Cl, was used as a poisonous chemical agentin World War I. Mustard…

A: Sulfur in mustard gas is more nucleophilic than other corresponding oxygen compounds. This is due to…

Q: NaOMe D. `Et nucleophile electrophile H3O+ E. F. 1. NaOMe Dieckmann Condensation OMe Meo 2. H30*,…

A:

Q: 1. НаNNH2, mild acid 2. КОН, Н20, heat 1. LDA 2. 3. Н,О, н* HCN KCN

A: Organic synthesis involves the process of preparation, isolation and characterization of organic…

Q: Write the complete stepwise mechanism for the reaction below: (Non-anonymous question Ⓒ) OH HC1 OCH3…

A:

Q: 1. CH3CH,MgBr 2. H2О 1. (CHз)2CuLi 2. H2о

A:

Q: Which of the following is a major product of the reaction sequence shown in the box? NABH4 HCI, H20…

A: Organic reactions are those in which organic reactant react to form organic products.

Q: CH3 PCC, CH,CI, reacting with

A:

Q: NH,NH2 of `NHNH2 pyridine H20 -ОН HO

A: The first reaction given is the reaction of acid chloride with hydrazine and the second reaction…

Q: If your product from this experiment (benzimidazole) is treated with a strong base (nBuLi) followed…

A: Benzimidazole is a fused ring in which benzene and imidazole are fused together. It is a…

Q: propose the mechanism for this transformation

A:

Q: 20) Provide the mechanism and draw the structure of the major product of the following reaction:…

A:

Q: a) Fill in the following scheme by drawing the missing reagents, intermediates and/or products.…

A:

Q: 1. Oxidation of alcohol CH;Cl2 CH;CH,OH + primary alcohol РСС ОН + CrO3 CH;CHCH3 secondary alcohol…

A:

Q: Provide a plausible arrow pushing mechanism for the reaction below. You may abbreviate the…

A: This is an example of Diels-Alder reaction followed by cyclization and aromatization.

Q: 1. СО» 2. H20, н* `MgBr 1. LDA 2. 3. НаО, н* -N 1. LIAIH4 2. Нао

A: The mechanisms are

Q: Propose an arrow-pushing mechanism for the following transformation. НО H30+

A: The above transformation is associated with the carbocation. In this transformation hydroxyl group…

Q: OH CH₂CNHCH3 CH3 C d OH CHCHNHCH₂ CH3 Ephedrine can be synthesized via reductive amination plus…

A:

Q: For each equation state the major reaction pathway that it will undergo. O Hold and drag to reorder…

A: The type of reaction to form major product can be determined by the reaction conditions.

Q: 3. Identify the products that will be formed when 2-heptyne reacts with each of the following…

A:

Q: Identify A, B, and C, intermediates in the synthesis of the five-membered ring called an α-…

A: In the synthesis of the five-membered ring alpha-methylene-gamma-butyrolactone , the 3 intermediates…

Q: 1. LIAIH4 2. H2О 1. LDA 2. 3. НаО, Н* NaBH4 MeOH

A: LiAlH4  is a reducing agent. It reduces imine to amine. LDA is a bulky base , it abstracts less…

Q: CH3 CH3 OH H3C CHS

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Propose a mechanism for the acid-catalyzed hydration of propene. Remember that a mechanism must…

A: Alkene reacts with water in presence of acid to produce alcohol.

Q: NO2 (а) Но

A:

Q: show the generation of the electrophile and predict the products.(a) benzene + cyclohexene + HF (b)…

A: (a) benzene + cyclohexene + HF=?  When benzene react with cyclohexene  in presence of HF to give…

Q: Complete the following reactions with SN1 + E1

A: Find the complete reaction mechanism as given below

Q: II] Propose a mechanism for each of the following reactions : Br 1) CH;OH OCH3

A:

Q: Use your knowledge of carbonyl chemistry and reaction mechanisms to explain the following biological…

A: Carbonyl group is an organic functional group which is composed of a carbon atom to doubly bonded…

Q: „coH COH

A: ANSWER > This is a radical reaction .In radical reaction the weaker the C-H bond, more readily…