H a A | MCPBA B PCC 0 1. Ag2O, NH4OH 2. Neutralizing work- up D LiAlH4 E OH DMP (Dess-Martin Periodinane) Done

Q: choose the correct reagent

A: In this question, we will see the reaction sequence for this conversion. So that, we can find the…

Q: Identify each compound as an ether, hemiacetal, or acetal.

A: Solution :       Ethers are one of the class of organic compound in which oxygen atom is attached to…

Q: Draw a stepwise mechanism for the following reaction. CH3 OCH3 CH3 CH3 Br CH,OH + + HBr CH3 CH3 CH3

A: Introduction :  We have to tell the products for the reaction .

Q: Match each reagent to the product that it forms. Multiple reagents may form the same product. Hoft…

A: Given are organic compounds made from same compound.The starting compound is secondary alcohol.

Q: 4. Complete the following reaction. reagent X HCN а) A в reagent Y b) OH

A: PCC oxidizes primary alcohol to aldehyde Grignard reagent converts ketone to tertiary alcohol HCN…

Q: Draw a detailed mechanism. For each step of the mechanism, jusiuny what you drew/explain the why…

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Q: Propose a suitable reagent.

A: Organic reactions are those in which organic reactant react to form organic products.

Q: Choose the correct product for the following reaction 4-methylcyclohexanone + Br2/H3O+ --> product?…

A: Answer:In this problem, given substrate is a ketone and we have to find out the product forming when…

Q: HO HC=CH

A: From acetyle The given compound have to synthesize .

Q: From cyclohexane and any other necessary reagents

A: Organic transformation

Q: 8) What reagent can be used to do the following reaction? a) KMnO/NaOH/H₂O b) Na2Cr₂O/H₂SO//H₂O c)…

A: The reaction of unsaturated primary alcohol gives a carboxylic acid product and the alkene group…

Q: Draw a stepwise mechanism for each reaction.

A: a) Please find below the reaction.

Q: UESTION 1 tify the reagents that you would use to perform the following reaction Br Br OH a. -b. OH…

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Q: Identify a reasonable starting material. NaCN

A: a) The first reactant is an alkyl fluoride which is (s)-3-fluorohexane and is shown below, The given…

Q: Choose the best reagents to complete the following reaction. Br ම

A:

Q: Draw a stepwise mechanism for the following reaction.

A: Please fine below the reaction mechanism.

Q: Acetals are formed from the reaction of two alcohols with a carbonyl under acidic conditions. Acetal…

A: During the acetal formation by 1,2-ethanediol and two molecules of ethanol, the same types of bond…

Q: Draw a stepwise mechanism for the following reaction.

A: SN1 mechanism :  It is a  Nucleophilic substitution reaction  where cabocation formation is the rate…

Q: HBr What is the major product of the reaction, ? E ther

A: The question is based on the concept of organic reactions.   We have to identify the product formed…

Q: 2·a-da CI

A: Firstly we can introduce the bromo(-Br) group at the allylic position of the benzene ring (left hand…

Q: Draw in the reagents for the following reactions and products. oxidant ロ→

A: The reagents for the following reaction are expressed as:

Q: Choose the correct product. 1. DIBAL H3CO ? 2. CH3OH H. ОН OH ОН H3CO H H H H3CO a b C d.

A: DIBAL is a strong, bulky reducing agent. It  reduces esters to aldehydes.

Q: 24. What reagent(s) needs to be added to complete the following reaction? A) N2O3 B) HNO3, H2SO4 NH3…

A: An aromatic compound reacts with the nitrating mixture to form a nitro aromatic compound. The…

Q: Draw a stepwise mechanism for the following reaction.

A: Reaction of Pyridine with Formaldehyde: Pyridine react with formaldehyde to give vinyl pyridine…

Q: Explain why two substitution products are formed in the following reaction.

A: Nucleophilic substitution reaction is a two-step reaction. A nucleophile is substituted at the…

Q: а) b) c) OEt

A: When aldehyde or ketone react with diol or alcohol it form acetal.

Q: Draw a stepwise mechanism for each reaction.

A: The nucleophilic substitution reaction involves the removal of the leaving group from the reactant…

Q: Draw a stepwise mechanism for the following reaction.

A:

Q: Starting with cyclohexanone and ethanol as the only organic reagents, use any inorganic reagents to…

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Q: H,0 Br KOCCH) LOH NaH LOTS TSCI pyridine Br TSOH NBS HBr

A: Here all step is nucleophilic substitution reaction and elimination reaction(SN2 and E2). So that…

Q: identify starting reagent

A: The objective of the question is to identify the starting reagent AcOH in the context of chemistry.

Q: a) Br OH b)

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Q: Draw a stepwise mechanism for the following intramolecular reaction.

A: In this reaction, HCO2H acts as a source of proton.

Q: OH OCH II CH2 CH3 CH он CH3 IV Which of the above is an acetal? OII O IV • Previous

A: An acetal is formed by the condensation of two alcohol and one aldehyde molecule.  An acetal…

Q: Starting from cyclohexanone, show how to make the two given products, include conditions to use in…

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Q: Synthesize each compound from the given starting materials.

A: Since your question consists of multiple subparts. So, we are solving only the first two. For the…