Q2/ Give the product for this reactions: 1) styrene + Cl; 2) Phenol + CH,COCI NaOH 3) Naphthalene + 5H; Ni

Q: sed on the reaction scheme below, draw the structure for compounds D, E, F (i) LIAIH4 in ether (ii)…

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Q: Q3. Let's try to suggest a synthesis for para-nitrotoluene from benzene, as shown below. CH3 ? NO2

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Q: What products would ypu obtain from reaction of 2,4-dimethyl-2-pentene with BH3, followed by H2O2,…

A: Alkene reactions with BH3 and H2O2 in presence of base are Hydroboration oxidation reaction.

Q: For each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2)…

A: The given alkyne is hex-3-yne. The alkyne on hydration in the presence of HgSO4/ H2SO4 gives…

Q: Which reagents react with an alkene by syn addition? Select all that apply. Incorrect selections…

A: The stereoselectivity during the addition reactions of alkenes leads to syn and anti-products. In…

Q: For each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2)…

A: The compound considered is a cyclic alkyne that has a 10 membered ring structure.

Q: Explain the following result. Although alkenes are generally more reactive than alkynes towards…

A: The given statement has to be explained.

Q: Ozonation followed by reductive workup of an alkene gave the following products. What was the…

A: Given :  products of reaction

Q: Give the major organic product(s) of the following. Include stereochemistry when applicable. 1) Nal…

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

Q: Draw the structure(s) of the major organic product(s) of the following reaction. 1. NaOCH3 / CH3OH…

A: Here we are required to predict the product of the reaction.

Q: 2. Propose a synthesis for the following molecules – should not take more than 5-6 steps. Hint: they…

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Q: Predict the product for the following: H TSO to -OTS OTS 1) LiAlH4 2) H₂O 3) TSCI, pyridine ?

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Q: NaSCH3 DMSO Mechanism Determine the anticipated ELIIMINATION mechanism for the reaction below. Using…

A: a) Here, substrate is secondary alkyl bromide and nucleophile is strongest that is NaSCH3 and…

Q: divls depends oin the moisture content of the reaction mixture. Propose a detailed mechanism for…

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Q: Draw the starting compound and provide the most probable reagent(s) to prepare…

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Q: Draw the structure(s) of the major organic product(s) of the following reaction. 1. NaOCH3 / CH,OH…

A: The hydrogen present in the alpha carbon of the carbonyl group is acidic due to the resonance…

Q: 1 eq HCI 50°C

A: There are two type of product is formed by adding of HCl in conjugated  diene..one is called kinetic…

Q: Which of the following reagents can be uşed to form an aldehyde from 3-methyl-1-butanol? [Note:…

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Q: Provide the structure of the product(s) with stereochemisty if appropriate. If multiple products…

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Q: Draw product (c) formed in the third synthetic step. Draw the molecule on the canvas by choosing…

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Q: Provide structures of products or starting compounds (A-D) for the following reactions. COOH KMNO4…

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Q: Draw the structure(s) of the organic product(s) predicted when this compound reacts with NABH4,…

A: NaBH4 acts as a reducing agent in organic reactions. In presence of carbonyl groups, the BH4-…

Q: Which Product(s) can NOT be the major (Markovnikov) product of water and sulfuric acid reacting with…

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Q: How many alkenes could you treat with H2, Pd/C to prepare methylcyclopentane?

A: In order to prepare methylcyclopentane by catalytic reduction 4 alkenes are requires. Alkenes with…

Q: Give the major organic product(s) of the following reaction. HO OMe ? + PCC Meo OMe

A: SOLUTION: Step 1: PCC (Pyridinium chlorochromate) is a mild oxidizing agent. It converts the primary…

Q: он Tso (9) Give the mechanism ? Is the alcohol acting as the as electrophile or the nucleophile im…

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Q: Give the major organic product(s) or reagents needed. Show stereochemistry Where approp OH K,CrO7,…

A: In organic reaction we can convert one functional group into other carrying out certain reaction…

Q: Nitration of Benzene with H,SO, will produce? O 1-Nitrobenzene O Dioxy ntrogen benzene O All O…

A: Nitration of benzene with H2SO4 will produce Nitrobenzene.

Q: How to synthesize trans-2-methylcyclohexanol from cyclohexanone?

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Q: Give the major organic product of the following reaction. H2 Ni

A: Hydrogenation of alkenes results in the formation of alkanes. It is an example of addition reaction.…

Q: Epoxidation is typically achieved by treating an alkene with: a. bromine b. NBS с. ТСРВА O d. BH3,…

A: Alkene reacts with each reagent differently to give different products. We will draw each product…

Q: Be the product of the reaction scheme below? TosCI NaNH(CH3) pyridine DMSO Na ONa

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

Q: For each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2)…

A: The expected product when the given reactant react with (1) HgSO4>H2SO4-catalyzed hydration and…

Q: SOCI2 pyridine РСС OH

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Q: 2. Provide products corresponding to the following reactions (remember to apply Markovnikov's rule):…

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Q: H,C-CC-CH, N-N N: CH3

A: Note: The above reaction is [3+2] cyclo addition. (See below).

Q: 1. H2SO4 Br +] H20 HO, NaBr 2. H3C-O H,C-O-Li Li f= Sn1 Nucleophilic substitution g= SN2…

A: The reactions given are,

Q: In the following multistep synthesis from butane to propanal, what reagent(s) would best install the…

A: Answer

Q: Propose a synthesis of the following: A) OH осн, но- B) CH, CH3 H3C OH H3C. CH H3C.

A: We are required to  design  synthesis for a certain chemical reaction using different reagent to…

Q: Propose a synthesis for the molecule. -CH3 N=C- NHCH₂CH3

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Q: Give two syntheses for (CH3)2CH¬O¬CH2CH3, and explain which synthesis is better

A: The given compound is ether. It can be synthesized by Williamson synthesis. The best yield is…

Q: Caper Give the starting alkene and regents needed to make the epoxide shown.

A: Note : Since you have posted multiple questions, we are entitled to answer the first only. Please…

Q: Q9:- Outine a possible laboratory, synthesis of each of the foliowing compounds from benzene and/or…

A: The answe to following question is -

Q: Provide the major organic product(s) of the following. H2SO4, A H3C CH3 ÓH

A: In presence of strong acids, alcohols undergo elimination reaction. Here elimination is preferred…

Q: as content is projected and Provide the reagents necessary to complete the following reactions. More…

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Q: Give the major product(s) of the following reaction. TSCI CH3CH2OH pyridine

A: This reaction shows tosylation of alcohols and alkyl tosylate has been formed as product.

Q: Starting with acetylene and 1-bromobutane as the only sources of carbon atoms, show how to…

A: Synthesis of  meso-5,6-Decanediol from  acetylene and 1-bromobutane as the only sources of carbon…

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.