Bromocyclohexane- Product in Step (i) i) Li ii) Cul iii) CH3COCHCHCH2CH(CH3)2 Product in Step (ii) Product in Step (iii)

Q: HN Can you draw the structure of the product for the followin 1) KOH 2) 3) KOH, A Br

A: Gabriel synthesis is used for the synthesis of primary amine from phthalimide when treated with…

Q: Rank the following alkyl halides according to SN2 reactivity. Put the most reactive compound at the…

A: To rank the given alkyl halides according to Sn2 reactivity.

Q: Estimate the AH reaction for the reaction shown below

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Q: O O O O Sn2 0000 Sn1 E1 E2 Br What is the major reaction pathway for the following reaction? Br ū E1…

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A: Grignard reagent provides a hard nucleophile and it gives a 1,2-addition reaction with the…

Q: Show all the steps necessay,in order to make each of the followring compoundS, Starting with benzene…

A: Preparation of 2,4-Dibromobenzoic acid from benzene can be done as follows:

Q: 21. The major product of the reaction shown here is A B Ja HCI Cy O

A: The objective of this question is to explain the chlorination by using hydrochloric acid .

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Q: Consider the following reaction. Which side is favored in equilibrium? u ů ^-^ 1 Selected answer…

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Q: What is the major product(s) of the first step (i.e. initiation step) of the following autooxidation…

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Q: In Williamson ether synthesis reaction, NaH plays both roles as base and deprotonation to alcohol.…

A: Williamson synthesis is an old method of synthesis of ether , using Sn2 reaction mechanism :…

Q: OH OH Ag2O Acetone

A: The reagent Ag2O is known as Fetizones reagent it is used for oxidation of aldehyde to carboxylic…

Q: How many intermediate/s is/are present in the reaction based from the energy diagram as shown below

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Q: What product will be produced in the following reaction? q Br a Br Br Br + HBr a Br

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A: Hydroperoxides (C-OOH) are formed when fatty acids undergo autooxidation in the presence of…

Q: Which reaction had the larger change in energy, the reaction with hydrochloric or acetic acid. Why…

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A: When an alkyl halide is treated with a strong base, the base abstracts proton from the C adjacent to…

Q: Rank the following alkyl halides according to SN1 reactivity. Put the most reactive compound at the…

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A: The carbonyl dichloride is known as phosgene. Due to the presence of two electronegative Cl atoms,…

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A: Pericyclic reactions are those reactions that occur in a concerted manner without producing any…

Q: of acyl halides and below showing 3. Reactions carboxylle derivatives . Dlease fill out acid…

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A: ->NaH is base which can abstract hydrogen and form alkene.

Q: 2. Draw the curved arrow notation and product for each of the C D SH HO. HO Hr

A: Given are organic reactions. These are acid-base type reactions. Here, one species abstracts proton…

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A: A question based on reactions of alkenes. An unsymmetrical alkene is given whose product on free…

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A: Benzoic acid react with sodiumbicarbonate gives sodiumbenzoate and carbondioxide and water.

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A: When an ether reacts with HCl, an alcohol and an alkyl chloride will be formed.

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A: We have to identify which compound will undergo SN2 reaction.

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A: These are the organic reaction, in which from two or more reactants it gives now product by breaking…

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A: DIBAL-H is selective reducing agent used specially for the reduction of ester into aldehyde.

Q: The structure shown below is has a very high pka because the conjugate base is very unstable. Using…

A: The treatment of cycloheptatriene with n-butyl lithium produces cycloheptatrienyl anion.

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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.