Select the major product of the following Diels-Alder reaction (assu

Q: What are the products of the following reaction. Explain.

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Q: 2. What is the E2 product of the following reaction and explain, using chair conformations, why this…

A: E2 elimination needs a strong base and the most important condition is the beta hydrogen and the…

Q: What product(s) is(are) formed in the following reaction Br/CH;Cl H Br plus enantiomer H3C Br Et Br…

A: When alkene is reacted with Br2 then cyclobromininum ion is formed as intermediate and then form…

Q: Draw all the possible products of the monochlorination of methylcyclopentane. Which ones are…

A: monochlorination of methylcyclopentane will bring Cl on the carbon in the methylcyclopentane  Since…

Q: Part: 0/2 Part 1 of 2 Draw the structure of one product that is formed in the reaction, including…

A: Alkenes when treated with osmium tetroxide (OsO4) form an osmate ester which on treatment with…

Q: Draw all stereoisomers formed when each alkene is treated with mCPBA.

A: Concept introduction: In presence of peroxide, alkenes are oxidized to epoxide. This reaction is…

Q: Br. CH3ONA H

A: The conformer structure for given structure is shown below.

Q: 1) ? 5- `N2 CI- 2) ? H,C. CH3 KMno, / OH- 6- ? heat

A: 1) Firstly reaction will occur with nanh2 then with diazotization process.  2) with KMnO4 the simple…

Q: Draw the alkene that would react with the reagent given to account for the product formed. ? + HCI…

A: Detail

Q: Draw the alkene that would react with the reagent given to account for the product formed. ? + H₂O…

A: Addition of water to alkene: Water adds to alkene to form alcohol. The addition of water is…

Q: 애 Conc H2SO4 스

A: Alcohols gets dehydrated in the presence of small amount of acid and heat to give alkene. The major…

Q: Draw the alkene that would react with the reagent given to account for the product formed. CH3 CH3…

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Q: (S)-Octan-2-ol Pyridine NaNg ) LIAIHA C MEOH II) H2O

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Q: e) 9-bromo 5-methyl 2-nonene -----H2, Ni 900°C---------- ? (name, str, stereochem) Cl2, CH2C12 f)…

A: Note: According to our guidelines we are supposed to answer only first three subpart . Kindly repost…

Q: Complete the following reaction by drawing the structure of the major product(s) expected. CH3 HCI…

A: The answer to the following question is-

Q: Two products are formed when methylenecyclohexane reacts with NBS? Show how each is formed.…

A: Allylic bromination :  NBS is a source of bromide radical .In presence of NBS allylic radical was…

Q: Draw all stereoisomers formed when each alkene is treated with mCPBA

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Q: What is the major organic product with the correct stereochemistry or geometry?

A: The given reaction is an Elimination reaction. The given alkyl halide will undergo…

Q: Please fill in the missing reactants, reagents or products in the following reactions. Indicate…

A: Lithium diisopropyl amide (LDA) is a strong bulky base. LDA reacts with an alkyl halide to form an…

Q: When carbonyl compounds are reduced with a reagent such as LiAlH4 or NaBH4 and a new stereogenic…

A: Since the carbonyl compounds have C in sp2 hybridisation  Hence the geometry of the molecule is…

Q: What is (are) the major organic product(s) obtained from the follow reaction? Br2 D…

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Q: a) OH type Bromination of an alcohol (Sn2) a) EtO₂C b) CO₂Et CO,Et b) OH c) type NH2 a) CN c) b)…

A: Note: Since you have posted a question with multiple sub parts, we will provide the solution only to…

Q: Draw the organic product of the following reaction. CH3 m-CICgH,CO;H • Use the wedge/hash bond tools…

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Q: Draw the sugar below in its open-chain form: OH НО- CH₂OH он OH

A: We have find out the answer.

Q: Draw the alkene that would react with the reagent given to account for the product formed. ? + H₂O…

A: This is reaction of alkene with H2O in presence of acid. In this reaction, first protonation is…

Q: OH HBr room temp. Br Br B Ol Br "Bri

A: The substitution and elimination reactions depend on the nature of the bulk of the incoming…

Q: 1-chloro-3-methylcyclopentane was reacting with 4. Optical active compound potassium t-butoxide in…

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Q: Are the products of the following reaction the same product (a single product that formed as a…

A: When oxygen donates its lone pairs to the proton, it results in the formation of an oxonium ion. In…

Q: Draw the structure for an alkene that gives the following reaction product. CH3 HCI CH3CHCH2CHCH3 ČI

A: Alkene generally gives Electrophilic Addition reaction, that is (i.e.) electrophile(electron…

Q: P33. Given the compounds above there are two variables you can test for an Syl reaction: The effect…

A: The rate of a SN1 reaction depends on many factors or variables. Steric hindrance, nature of…

Q: Draw the alkene that would react with the reagent given to account for the product formed. ? + H₂O…

A: The addition of water to alkene in presence of sulphuric acid is by markonikov's rule. Markonikov's…

Q: Two products are formed when methylenecyclohexane reacts with NBS? Show how each is formed.…

A: N-Bromosuccinimide (NBS) is a reagent used for the bromination of allylic hydrogen atoms.…

Q: 1) ВНз-THF А. 2) NaOH, H2O2 H2 В. Pt

A: The racemic mixture form from both the enatiomeric form present in the same compound. Generally…

Q: optically active 2- butanole slowly becoms racemic whem treated with with dilute acid > explain why

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Q: Classify the pericyclic reaction and indicate how many bonds broken/formed. + Cycloaddition

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Q: Explain the Types of Pericyclic Reactions ?

A: A pericyclic reaction is an organic reaction where the transition state has cyclic geometry and 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.