3. This target alcohol can be made in a two-step synthesis from each of the starting materials shown. Show the steps. OH target OH Any of these starting materials

Q: CH3CO3H

A: In presence of per acid ,ketone molecule undergo Baeyer villiger rearrangement. Among two alkyl…

Q: reagents in the correct order for the synthesis of the target molecule?

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Q: Which set of starting materials can be used to make the target molecule in one step? HO. Но Target…

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Q: OH BrCH2 COCH, CHCHN Co,CH heat The synthesis of this morpholino derivative occurs in several steps.…

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

Q: NO2 NH2 Br NO2 НООС b. NO2

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Q: Chemistry complete the synthesis mechanism, show each step H,N

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Q: For the reaction shown, draw the transient product of one equivalent of reagent adding across the…

A: Alkyne gives alkene and futher alkene reduces into alkane on catalytic (Pt /Ni/ Pd) hydrogenation.

Q: Drag the appropriate labels to their respective targets

A: The left hand side boxes consists of two boxes which i marked as 1 and 2 from up to down- 1, Fusion…

Q: Which product(s) will be formed preferentially in a base elimination? (1) (2) H KOH, EIOH Br Br (3)…

A: Ans

Q: Using retrosynthetic analysis, design a synthesis of the following target. HO Br Target

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: NaCN Dimethylformamide

A: The above reaction is an example of intra molecular Benzoin-condensation reaction.

Q: Complete the mechanism for the reaction of butanone with NABH, followed by the addition of aqueous…

A: When a ketone is reduced with sodium borohydride and acidic hydrolysis, then ketone is changed into…

Q: OH HO Br HO

A: The question is based on the concept of chemical conversions. we have been given reactant and…

Q: Drag the appropriate labels to their respective targets. Note: not all labels will be used. pK. <0…

A: pKa is known as the dissociation constant of an acid how easily the molecule or the compound can…

Q: Draw curved arrows to illustrate the mechanism for the reaction of 3-methylbutan-1-ol and HBr. The…

A: Alcohols react with HBr to produce alkyl bromides. It may be noted that secondary and tertiary…

Q: 1. Indicate if the reaction is Felkin-Ahn or Cram and Chelation model. 2. Show Newman Projection…

A: since you have posted a question with multiple subparts, we are entitled to answer only first three…

Q: SH 5 steps

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Q: In the SN2 reaction shown, identify the actual species that will serve as the nucleophile that will…

A: The replacement of any atom or group of atoms in a molecule is termed as substitution reaction.

Q: Fil in the blank with the reagents necessary to complete the synthesis shown Drag the appropriate…

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Q: 3. Show the step(s) necessary to carry out this transformation: cyclohexanone →…

A: When ketone react with primary amine then it forms immine. It is formed under acidic conditions.…

Q: II Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…

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Q: Complete the mechanism and draw the final product for the Grignard reaction. Step 1: Add curved…

A: Grignard reagents undergo a reaction with epoxides and lead to the formation of alcohols. The…

Q: TM H Show the synthetic sequence that converts acetylene to the target molecule (TM) shown below.

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Q: of KOH / CH;OH HO,

A: Organic reaction mechanisms:

Q: Draw the major product of the reaction sequence. Omit byproducts. 1) C,H, MgBr, then H,O* 2) H, SO,,…

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Q: Using the Strecker Reaction, please show the steps and the final product of the following reaction:

A: Strecker synthesis is preparation of alpha- aminonitriles which are intermediate for the synthesis…

Q: Design a synthesis to accomplish the following in two or more steps. steps Bno.

A: 1. Reduction of Lactone with DIBAL-H.2. Condensation reaction of H2H(n-Pr) with the aldehyde.3.…

Q: Draw the product of the attached reaction:

A: Product of the above reaction is given below,

Q: Please finish this mechanism problem and show all movement of electrons and any thing you used to…

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Q: Construct a three-step synthesis of 1-bromopropane from propane by dragging the appropriate formulas…

A: The reaction of alkane with bromine in presence of sunlight undergoes substitution reaction. This…

Q: H3C I NaOH Меон, 82 °C

A: Sodium hydroxide abstract the proton forms carbanion. The formed carbanion forms alkene with…

Q: Which reaction steps would you use to carry out the synthesis shown? phmylacetyieme 1. Na/NH3;…

A: here 1-alkyne react with base , base abstract the proton of alkyne and formed negative charge  2-…

Q: Rewrite each of these transforms as a synthetic step in the forward direction, including reagents…

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3 sub-parts. Please resubmit the…

Q: Arrange in increasing order the following compounds/ substrate with respect to both SN1 and SN2…

A: A question based on the reactivity of substrate to SN1 and SN2 reactions, which is to be…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…

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Q: Challenge Problems: use these pathways and other reactions to complete the below synthesis problems:…

A: The conversion of the given compound to the desired product can be obtained by reacting them with a…

Q: Arrow-pushing Instructions MeOH Draw curved arrows to show the movement of electrons in this step of…

A: Given reaction is :  Draw the curved arrows to show the movement of electrons in this step of the…

Q: CI HC1 CH;CHCH3

A: Answer: Propene (CH3-CH=CH2)

Q: 1) PhMgBr 2) H2O

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Q: Construct a three-step synthesis of 3-bromo-3-methyl-2-butanol from 2-methyl-2-butene by dragging…

A: Reactant molecule is 2-Methyl-2-Butene and product molecule is 3-bromo-3-methyl-2-butanol.

Q: Shown in the figure is the synthesis of several compounds starting from an aldehyde. Identify the…

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Q: 12. Show the starting materials you would use in the Suzuki reaction in order to create target…

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Q: 1. CH3CH2MgBr 2. НзО*

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Q: Design a synthesis for the following reaction. If more than one step is needed, be sure to number…

A: Here we have to convert but-1-ene to butanoic acid in multistep reactions.

Q: Carefully draw the mechanism of the following reaction using arrows to show the movement of…

A: The given reaction is an example of Electrophilic Bromination of Benzene.   This reaction occurs in…

Q: Construct a three-step synthesis of trans-2-pentene from acetylene by dragging the appropriate…

A: Given scheme,

Q: In the reaction below, the hydroxide ion serves as the: CH3CH₂C O Base o Nucleophile O Leaving Group…

A: The given reaction is  an example of nucleophilic substitution reaction. One nucleophile substitutes…

Q: HN- H. CO-H. -Zn2+ NH2 N. N. HO 4 N.

A:

Q: Draw the product of the reaction. 2 equiv. HO, H*

A: A question based on organic reaction, which is to be accomplished.

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.