Q2/ What is the major E2 elimination product formed from each halide? CH H. CH 3. b. CH CH, CH,CH, CH,CH,

Q: Draw a stepwise mechanism for the attached reaction.

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Q: H OTos С. d. a. b. H OTOS H OTOS

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Q: Draw the products of each reaction. [1] SOCI2 [2] (CH3CH2),NH (excess) SOCIl, a. b. он CH3CH2 HO

A: The product of the following reacts, (a) (b)

Q: What is the product of the E2 reaction below? CI KOC(CH3)3 ??? A O A O B

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Q: Draw the product formed by treating each compound with excess CH3I, followed by Ag2O, and then heat.

A: The complete reaction for a is shown below.

Q: Draw the product formed in each reaction. [1] NANO2, HCI [2) CuBr [1] NaNO2, HCI [2] HBF, -NH2 c.…

A: Since you are posted with multiple sub-parts. As per the rule, I am answering the first three…

Q: Draw a stepwise, detailed mechanism for each reaction.

A: Please find below the reaction mechanism for the reaction 1.

Q: Draw a stepwise mechanism for the following reaction.

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Q: What reagent is needed to complete the following reaction? B None of these A U CH3 CH3I (A) ??? IN 3…

A: Here nucleophilic substitution occurred, I- is the leaving group , so  N3- is the nucleophile. Hence…

Q: What is the major E2 elimination product formed from each alkyl halide?

A: Elimination reaction are those reactions which elimination occur with removal of small molecules…

Q: Draw a stepwise mechanism for the following reaction. HBr HO. Br + H20 Br +

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Q: Draw a stepwise mechanism for the following reaction.

A: Since on reaction with the H2SO4 , the OH group will take a proton from the H2SO4 and leave as water…

Q: Draw the product of each reaction.

A: Cyclic ketones can be converted into 1,2 or 3 degrees amines using reductive amination. In the above…

Q: Draw the most stable form of the major mixed Claisen product formed in the following reaction. 1.…

A: Step 1:  Extraction of acidic hydrogen from ethyl acetate takes place not from ethyl isobutyrate due…

Q: 9.49 Draw a stepwise mechanism for the following reaction. Он H,SO. H20

A: Major Product:- Major product will be 1-methylcyclopentene. Because there are 3 substituents on this…

Q: Draw the product of each reaction. NH3 (excess) -NH2 CH3CH,Br (excess) a. b.

A: Draw the product of each reaction, (a) (b)

Q: Draw a stepwise mechanism for the following reaction.

A: Please fine below the reaction mechanism.

Q: 2. Which reaction will proceed faster A or B? CI H2S H2S 'CI A B

A: If i draw these molecules in chair conformations and lock t-butyl groups at equitorial position for…

Q: Draw the product of each reaction.

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Q: Draw the alcohol product expected from each reduction reaction. CH;CH,CH,C–H + H, *, Pt…

A: Carbonyl compounds can be reduced into alcohols. The aldehyde reduces into primary alcohol and the…

Q: (a) Draw the intermediate product resulting from the arrow movement in compound A. (b) Circle the…

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Q: 6. Draw the prod uc ts formed from nitration of each compound OH он b. CH3

A: Two aromatic structures whose nitrated product is to be reported.

Q: Name each epoxide: CH3 a. b. (two ways) H (wo ways) CHá

A: Answers are explained below.  Epoxides are named in three different ways those are oxiranes,…

Q: Draw a stepwise mechanism for the following reaction.

A: CrO3+H2O+H2SO4- The mixture of CrO3, H2O and H2SO4 is called as Jones reagent. Jones reagent is…

Q: Draw the product of each reaction

A: Finding: To find the product of the following Reactions (a) & (b):

Q: H CH3 Pt С—С H-H H3C H +

A: Hydrogenation of alkene: Alkene can be hydrogenated by the reaction with hydrogen in presence of a…

Q: 2. Draw the products of each reaction. CH;CH,CI b. HNO3 -NO2 Cl2 a. OCH3 Br с. AICI3 H,SO4 FeCl3 3.…

A: 2. (a) The given reactant is anisole. It undergoes Friedel-Crafts alkylation reaction with CH3CH2Cl…

Q: FOLL Eto OEt 1) NaOEt 2) 3) H₂O* OEt

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Q: Draw the major product formed in attached reaction

A: Amine being a nucleophile can react with the alkyl halide. When an excess of CH3I is added to a…

Q: What products are obtained from the reaction of the attached compound with one equivalent of Br2,…

A: The reaction with Br2, using FeBr2 as a catalyst causes the electrophilic aromatic substitution…

Q: Draw the substitution and elimination products.

A: Hey since you have posted a question with multiple sub-parts, we will solve first three sub-parts…

Q: Draw compounds B and C from the following reaction scheme. excess CH3I Ag20, H20 heat A B

A: In presence of excess of CH3I followed by oxidation by silver oxide, amines undergo Hoffmann…

Q: Label the α and β carbons in attached alkyl halide. Draw all possible elimination products formed…

A: Biomolecular elimination (E2) reaction: E2 reaction involves a one-step mechanism in which…

Q: C. any additional reagent Show one different routes in the Grignard Reaction OH The

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Q: kill 8.39 Identify the reagents y (a) tneo leirb benistdqainemojpene no nerW (c) Enema noitso

A: Since you have posted a question with multiple sub- parts, we will solve first three sub- parts for…

Q: Draw the more stable enol for each structure. hoo000.000

A: the solution is as follows:

Q: Which alkyl halide in each pair is more reactive in an E2 reaction with hydroxide ion?

A: Since in E2 reaction, the reactivity is  primary alkyl halide < secondary alkyl halide <…

Q: Label the α and β carbons in attached alkyl halide. Draw all possible elimination products formed…

A: Dehydrohalogenation Reaction: The secondary halide undergo either elimination or SN2 depending upon…

Q: Ethers are oxidized with O2 to form hydroperoxides that decompose violently when heated. Draw a…

A: The above reaction takes place via a free radical mechanism.

Q: c) Draw the major product(s) for each reaction. 1. Sia,BH 2. Н,О2, NaOH Na, NH3 3-hexyne (c) xs I2…

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Q: Which halide in the attached marine natural product reacts fastest inthe SN2 reaction?

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Q: Draw the enol form of each keto tautomer in parts (a) and (b), and the keto form of each enol…

A: Keto-Enol tautomerism is an equilibrium that exist between carbonyl group (aldehyde and ketone) and…

Q: Draw the keto tautomer of each enol.

A: Tautomers are isomers of a compound which differ only in the position of the protons and electrons.

Q: What is the product of the following reaction? Circle the correct answer. NABH, A. B. C. D. Он О Он…

A: The reagent "sodium tetrahydroborate (NaBH4)" works as reducing agent. The ketones and aldehydes can…

Q: Draw a stepwise mechanism for the following reaction.

A: Given reaction,

Q: OPICH5)3 H Br 1. P(CH5)3 () (H or) R చం R. (or H) 2. R-Li R R (or H) (or H) Alkyl halide Wittig…

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Q: Label the α and β carbons in attached alkyl halide. Draw all possible elimination products formed…

A: The dehydrohalogenation takes place in accordance with the Saytzeff's rule, according to which the…

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.