accomplish

Q: Complete the following synthesis schemes. Some may take more than one step and some may have several…

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Q: `OH

A: In given reaction   , alkene is converted into alcohol.

Q: OH HCI

A: Answer :- Keto enol tautomerism :-  Keto enol tautomerism observed in carbonyl compound containing…

Q: B) Show step by step reactions to carry out following transformation.

A: The conversion taking place is given as,

Q: Explain why the following reaction sequence will not occur: + + NH3 NH3 AICI3

A: We have to explain the following given reaction sequence will not occur as follows in step 2:

Q: From each pair, select the stronger nucleophile. Q.) CH3OCH3 or CH3SCH3

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Q: Identify the reagents that vou would use to accomplish each of the following transformation:

A: The transformations are given below -

Q: (CH3)3SICI ZnCl2

A: Synthesis and reaction of enolate.

Q: (CH3),CCI ?

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Q: Он CN

A: This conversion can be done in 3 steps: 1. Conversion of cyclohexene to cyclohexanol, 2. Conversion…

Q: F CH2CH3 B-F H3CH2C-o F

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Q: Indicate the reagent needed for the below reaction: н он

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Q: Rank the following in terms of reactivity towards a nucleophile (1 = least reactive and 4 = most…

A: Electrophiles are reagents that are electron deficient. These attack reagents that are rich in…

Q: Please give the reagents that will perform the following reaction.

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Q: This will require more than one step of reagents to arrive at the final product. Write the…

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Q: Please identify major PRODUCT A and major PRODUCT B.

A: We have given the organic reaction and we have to identify major PRODUCT A and major PRODUCT B

Q: G. Н. I.

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

Q: Draw out the complete mechanism of the reaction and include all relevant electrons and arrows…

A: It is given that in the reaction benzaldehyde and acetone are the substrates which are undergoing a…

Q: Which compound will be a major product of the reaction sequence shown? NO2 NO2 (1) HNO 3/H,SO,, A…

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Q: propose a synthetic route to this structure that includes at least one C-C bond formation step.

A: 2 -Methylbutanoyl chloride can be synthesized as given below.

Q: 6. Br2, aq. NaOH `NH2 1) LDA 7.

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Q: A B гон NO2 но D

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: Arrange the intermediates below in order of increasing basicity:

A: The basicity is ability of species to accept proton. More the acceptance of proton, more is basic…

Q: Which of the following is most prone to hydration (acid-catalyzed reaction with water)? a. b. C. d.…

A: Aldehyde which is most prone to hydration is.

Q: Complete the Reaction below by providing both major and minor products, circle the major product.…

A: Given reaction is :  Complete the reaction and provides the major and minor products ?  The given…

Q: 1) Propose an efficient synthesis for the following Transformation. **You can only use the…

A: Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: A. Propose a short synthesis for the following molecule. You can start with acetylene, and alkyl…

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Q: Propose a mecahism for the following reaction and include all relevent reagents (you may use any).…

A: This is a multi step synthesis reaction . By using the starting material with various reagents we…

Q: c) Propose a mechanism for this reaction. BF3 Но HO.

A: BF3 , boron triflouride is lewis acid. So lone pair of oxygen of -OH group attack on it and…

Q: Provide the appropriate reagent(s) for the following transformation.

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Q: Provide the appropriate reagent(s) for the following transformation

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Q: Define how Polar protic solvents and polar aprotic solvents affect the rates of SN1 and SN2…

A: Nucleophilic substitution reactions are the reaction in which nucleophile replaces the leaving group…

Q: Provide the necessary reagents next to the arrows.

A: Benzene is an aromatic compound as it has π-electron cloud. It will undergo electrophilic…

Q: Complete the following reactions with the missing reagent(s) or major product(s)..

A: Alkane is treated with Br2/hv it gives alkyl bromide via freeradical substitution Alkylbromide in…

Q: NaOH N2OCH3 H3CO OCH heat

A: "Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: Write the correct mechanism and major product for a), and indicate the reagent needed for b) to…

A: Two question based on alkenes, which are to be accomplished.

Q: a) ホ→ OMe b)

A: Number of functional group is associated with organic compounds which impart specific chemical and…

Q: Perform the following transformation and propose a mechanism Br ОН Br НО

A: When alpha-bromo ketone reacts with NaOH then to get carboxylic acid is formed. This is called…

Q: Draw compound A and B and identify reagents 1,2 and 3

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Q: PROPOSE AN EFFICIENT SYNTHESIS FOR THE GIVEN TRANSFORMATION

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Q: Br Br2 OH

A: In the given reaction, the first step of the reaction is the addition of the bromine to the double…

Q: B. Give a reasonable synthesis pathway for the transformation below. You may use any organic and…

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Q: Provide the reagents necessary to complete the following transformation. CH, -CH3 to

A: free-radical halogenation (more substituted alkyl halide is formed) E1 elimination  acid catalyzed…

Q: Select the arrow drawing that best describes this step of an E1 reaction. H I-0: І H3C I нн i 1-0:…

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Q: Carry out the following reactions by showing the step by step transformation. More than one step may…

A: All the given transformations involves two steps and different reagents are required to carry out…

Q: Propose an efficient synthetic route for the following transformations:

A: We can prepare this molecule by Michael addition reaction.

Q: H2SO4 +

A: The reaction taking place is given as,

Q: Multistep Syntheses: Draw all the reagents as well as the major product of each step necessary to…

A: Given starting material is beta, gamma unsaturated carbonyl compound and name of the compound is…

Q: For each case below, explain why those are the favored mechanisms Strong bulky bases (primary and…

A: In E2 elimination reaction,  base has to come and accepts proton and that electron is push back ,and…

Q: Complete the following reactions with the missing reagent(s) or major product(s).

A: Solution: We can see this is the step down reaction in which given molecule is break down into two…

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.