CH3 Na/CH3ОН NH3 (liquid)

Q: Select the major product of the reaction sequence below. CH,CH2CH3 H,C CH2CH3 Br 1. KOH/ 200°C 2.…

A: The details solution for this is provided below in attach image.

Q: с. H2N° HO, SOCI2 (еxcess) N-CH3 CH3

A: Detail mechanistic pathway is given below to find out the final product

Q: Alkyl halide that gives ONLY one alkene as the product in the E2 reaction is Select one: a. Br Ob.…

A:

Q: appropriate H3C CH3 Br КО-+-Bu ID НО-+-Bu a. CH3 NaOEt b. Ph-c -Br CH3 c. Show the curved arrow…

A: In the two reaction, the first one is an elimination reaction. Second one is nucleophilic…

Q: What is most likely the first step of this reaction's mechanism? CH CH;CH,OH Br CH3 Br CH;CH2O- CH3…

A:

Q: What is the product of the following two-step reaction sequence? Br2 Na CH3C=CCH3 NH3 H CH3 H2N, H3C…

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Q: H3C. КОН, Н-О CH3 H

A: Organic reaction mechanisms SN1 reaction mechanisms.

Q: 3. Provide the mechanism for the following rxn: ethanol heat Br a. CH3 CH3 NAOCH3, CH3OH Br b. DH H.…

A: Mechanism of Elimination reaction:

Q: Select the major product of the reaction sequence below. OH OH CH,CH,CCN CH,CH3 CH,CH,CCH,CH, CO,H B…

A: Acyl chlorides are also called acid chlorides, with the general formula of RCOCl, the R represents…

Q: Which pair of reactants is most likely to undergo an E1 reaction? O CH3SNa + (CH3)2CHCH₂CH₂CH₂Br at…

A: E1 (unimolecular elimination) is a reaction where there is a loss of the leaving group followed by…

Q: 6.) Provide a reasonable mechanism, including all curvy arrows and intermediates, for the following…

A: Fluroine when attached with aromatic ring becomes a better leaving group. Fluorine is having…

Q: 3) Write a detailed mechanism of: CH, CH. HNO" H'SO O,N

A:

Q: Arrange the following compounds in their ease of undergoing an S,2 reaction: a) СЗСН2СH2-CІ b)…

A: For substitution reaction, nucleophile has to attack from the back side of the leaving group in the…

Q: II] Propose a mechanism for each of the following reactions : NaOCH3 Br 2)

A: Here i have explained the mechanism of this reaction

Q: CI 2HCI CH3-CECH CH3-C-CH3 CI

A:

Q: Br CH3-CEC -CH3 2HB1 CH3-Č-CH2-CH3 + Br

A:

Q: Br 1) NaOH / 70 °C 2) H30° NO2

A: This is aromatic nuclophilic substitution  reaction.

Q: Select the major product of the reaction sequence below. OH NHČCH, NHCHCH, NHCH,CH, NHCHCH, NHCH,CH,…

A: Step 1: Fridel Craft's Acylation at the para position.Step 2: Reduction of amide and ketone group to…

Q: Which of the following SN2 reactions proceeds the fastest? NaSCH3 CH3-CH2-CH2-Br DMSO NaOCH3…

A:

Q: The SN2 reaction proceeds with 100% inversion of configuration as a consequence of backside attack…

A: SN2 - Nucleophilic substitution bimolecular reaction.  In SN2 reaction the rate of the reaction…

Q: cat. A + cat. B .R + 2 R H3C-CH3 R

A: Catalysts are the substances that facilitate the occurrence of a chemical reaction. The reaction…

Q: Which compound is a major product of the reaction sequence shown below? (1) benzene COOH ..COOH OCH3…

A: Major product

Q: Provide a complete mechanism for the following reaction. Use curved arrows to depict electron each…

A:

Q: CI HCI H3C CH3 H2C CH3 H3C CH3 CI CI H2C CH3 CH3 H2C CH3 ČI Treating 1,3-pentadiene with one mole of…

A: Product.

Q: Which synthetic method below correctly does the following conversion? СНО СНО Br A) (1) Mg, diethyl…

A: When aldehdye undergoes a reaction with alcohol, acetal is produced. When alkyl halide undergoes a…

Q: er: HBr CH3 CHa CH2 CHa Br CH3 CH2 CH2 CH2 Br + Hao

A:

Q: In which solvent is the following reaction faster? t-BuBr + CH3OH ethanol DMSO

A:

Q: ce CH3 -CH= CHz Cez CH3 - CH2 CH CH2Clz Cん

A: This is electrophilic addition reaction. Here propene reacts with chlorine through a cyclic…

Q: CH,=CH-C-CH3 ОН CH3-CH2-CH2-C-H CH;CH3

A: Base used for formation of enolate (nucleophile).

Q: 2. Propose a complete and accurate arrow pushing mechanism for the reaction below. HNO3 H2SO4 O2N 3.…

A: Nitration: It is the chemical reaction in which there will be the addition of nitro group (NO2) to…

Q: 3) write a detailed mechanism of: HO -OH CH3ČCI AICL3 CCH3

A: The reaction of phenol with acetyl chloride in the presence of anhydrous AlCl3 to form…

Q: Which product will be formed from this E2 reaction ? CH2C H3 H. CHCH3 H CH2CH, base CH2CH3 CH2CH3…

A: given  one E2 reaction

Q: For the nitration of a monosubstituted benzene, which substituent, when attached to benzene,…

A: We add conc HNO3 and conc H2SO4 to bring about nitration in each of the species.

Q: 5. Please write out the mechanism for the following reaction (Note: SN1) CH;OH CH3 Br OCH3

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Q: 2. Give a stepwise mechanism for each reaction (i) OH 1) CH;MgBr (excess) 2) H2О (ii) OCH3 „NO2 N-…

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Q: The major product that would form during the alkylation reaction shown below is? Br. A. B. OC. D.…

A: A question based on introduction to organic chemistry that is to be accomplished.

Q: A set of three nucleophilic displacement reactions is shown below: CH3 CH3 CH3Br CH;CHCH2CH2B1…

A: The correct answer about SN2 reaction is given below

Q: 1. Complete the following reactions: 1. Hg(OAc);/H,O CH3CH2CH2CH=CH2 2. NaBH4 CH3 1. Hg(OAc);/H;O 2.…

A: Following reaction are named according to the reagent used in the reaction which is mentioned with…

Q: The product of the following reaction sequence is: 1. NaOCH, CH3OH 2. CH3 3. H3O*, A (a) (c) CH3…

A: The reagent sodium methoxide is a base that abstracts proton resulting in the formation of…

Q: Select the major product of the reaction sequence below. O CH, O CH,CCHCHCH,CCH, A CN CH,CH=CHCHCCH,…

A:

Q: Br (CH3)COK + CHB13 Br (CH3);COH

A: Singlet- Carbene :   This Carbene  has a lone pair of electron for donation again , it has a vacant…

Q: 3) Circle the compound undergoes faster solvolysis (SN1) in ethanol. Br Br Br c) Br Br Br b)

A:

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

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Q: CH3 CH3 Br FeBr3. HBr (а) Br2 ČH3 CH3

A:

Q: Which of the following SN2 reactions occur faster and why? a CH3 H2 -C-Br CH;CH,CHBr + OH or H,C-…

A:

Q: 1) NaOEt / ETOH 2) H300 +

A: The question is based on the concept of organic reactions. we have to identify the product and…

Q: Propose a mechanism for the following reaction:

A: The mechanism for the above reaction has to be proposed below.

Q: 3. Show a mechanism for the following reaction. 8-x-8 OH NO₂

A: Answer : General Reactions :     The 2-chloro-5-methylphenol and 3 fluoro-6-nitroanisole to formed…

Q: CH3 o-nitrotoluene CH3 NH, CI NO2 CH3 o-toluidine NH3*,CI CH3 CI 2-chloro-N-o-tolilpropanami NH,HCO,…

A: The solution is given below:

Q: 1. Excess LIAIH4 MeO НО 2. H2о

A: Given reaction: We have to write the mechanism of the reaction.

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.