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Q: A D H,O* CH,CI H,SO, H;C B E KMNO, + + HNO, H AICI, AICI, A Cl, FeCl, F+G 7. Based on the reaction…

A: (7) (a) Structures of compounds A to H are -

Q: Would heating each of the following reactions increase the yield of the product shown? (a) (b) NAOH…

A: When a reaction mixture is heated, the reactions which needs heat for the product formation have…

Q: 21.96 A student treated methyl 2-methylpropanoate with sodium methoxide dissolved in methanol. After…

A: a) When methyl 2-methylpropanoate is treated with sodium methoxide in methanol , the expected…

Q: 1) Consider the acid-base reaction below. A) Predict the products and show the arrow-pushing…

A: The reaction between propanoic acid and sodium ethoxide gives sodium propionate and ethanol. The…

Q: hydrocarbon c8h10 is heated with acidified potassium manganate. c7h602 is obtained. 1) how p is…

A: The compound with the formula C8H10 is likely to be an alkene, given the presence of a double bond…

Q: In attempting to make 2–bromo–2–methyl–propane from 2–methyl-propene, as shown below, you used a…

A: Interpretation - We have to tell about the mechnaism of unwanted by-product formation in the avobe…

Q: Consider the reaction scheme shown below. HCI [1] HO. (a) Provide a detailed mechanism for reaction…

A: This reaction will occur via 3 step. In first step protonation then Water molecule eliminate to…

Q: Br HI (1 eq.),

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Q: Give detailed Solution with explanation needed

A: Wittig reaction is the formation of alkene from aldehyde and ketones. The reagent used for the…

Q: ) Provide a reaction mechanism for the following reactions and name the major product for each. HBr…

A: SOLUTION: Step 1: 2-methyl-2-butene reacts with HBr to form 2-Bromo-2-methyl butane as a major…

Q: Establish the reaction and propose a mechanism for the reaction of benzene with bromine catalyzed…

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Q: (v) Provide a detailed mechanism for the Claisen reaction between S and T, and give the structure of…

A: We have to give the mechanism for the Claisen condensation reaction takes place between the compound…

Q: For each reaction, draw the complete mechanism and the major organic product(s), paying attention to…

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Q: 5. Draw the mechanism and show the products with correct stereochemistry (a) OTS (b) Br OH + CH₂OH ?…

A: The objective is to complete the given reaction and find the product formed. Tertiary alkyl halides…

Q: Ⓒ CH3 + H₂O₂ (d) product from part (c) heat

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Q: The following conversion, carried out in the presence of Grubbs catalyst and ethylene gas, involves…

A: The indicated atoms are labeled as 4, 8 and 13 in starting material. It is intramolecular reaction.…

Q: Propene reacts with hydrogen bromide to form two isomers, the major product being 2- bromopropane.…

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Q: (d) Complete the following reaction (with mechanism) : Ph Ph + MeNH, NaBH4 EtOH, A ? 3

A: Methyl amine acts as a nucleophile and attack to the carbonyl carbon . NaBH4 acts as a reducing…

Q: (b) Propose a mechanism for the following reaction, with curved arrows to show bonding changes. OH…

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Q: is the reaction possible? predict the product and show reaction mechanism

A: Hydrolysis of ester gives carboxylic acid as product.  Acidic hydrolysis of an ester gives a…

Q: (b) Addition of HBr to the alkene in the presence of peroxide form radical intermediates. Based on…

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Q: Consider the following reaction. Br Br excess NaOH Only one bromine atom is replaced 50 °C O2N `NO2…

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Q: B OH A OH NaH PBr3 C D F (a) Name the functional groups in compounds A, B and F, including, if…

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Q: (b) How can be prepared from OEt CO,Et and at EtO OEt EtO2C 95 °C ? Provide the mechanism.

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Q: Instructions: Write ONE mechanism for the indicated reaction. Include all intermediate, formal…

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Q: ОН

A: These reactions are generally proceeds in a heating or light conditions.  Here we are given with…

Q: Give the major product of the monobromination of n-butane (or butane) in the presence of light or…

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Q: Write the products of the following reactions and give the mechanism of each reaction. (a) J (b) (1)…

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Q: Write the product and mechanism for hy

A: Given substrate is 1-(but-3-en-2-yl)-4-methylbenzene. In the given substrate we have a 1,4-diene.…

Q: (a) Identify the major product of the following reaction. (b) Explain why the other product is not…

A: a) The major product is (II). b) The reaction is followed the mechanism of Friedel-Crafts…

Q: Explain and detail the reaction mechanism: NaBr + H2O + n-butyl alcohol = ?

A: In this que, acidic condition is missing, this reaction cannot take place in absence of acidic…

Q: (a) Name the reactant (including E/Z configuration) and draw the structure of the major product for…

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Q: vi) please

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Q: 2. Predict the organic product from each of the following reduction reactions. (a) O OH OMe NaBH4 A…

A: NaBH4 ---> Reduces aldehyde and ketone to alcohol NaAlH4 ---> Reduces aldehyde, ketone, ester…

Q: NaoCHy CH, ON A

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Q: (b) 2-Ethylcyclohexanol, on treatment with hydrobromic acid, gives 1-bromo-1- ethylcyclohexane.…

A: Hydrobromic acid is a strong acid that dissociates to give H+ and Br- ions in solution. It is used…

Q: Draw a multi-step mechanism for this reaction and predict the structure of the organic product.…

A:

Q: Mechanism: Provide the mechanism for the following reactions. 1) NaOEt 2) Hао

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Q: Give to all parts?   (a) Give the complete mechanism for the reaction of trans-2-butene with Br2…

A: In the reaction of alkene with Br2/H2O, the major product is halohydrin.

Q: (b) Provide a detailed synthetic route (steps including reagents) for the synthesis of alcohol 5…

A: The reactant given is known as 5-oxopentanoic acid and the product is called…

Q: Explain  the Mechanism - Addition of Dichlorocarbene to an Alkene ?

A: Carbenes are short lived intermediates. Therefore, they are mostly prepared in situ, during the main…

Q: + H2O CI Based on the reaction above, (a) Outline the reaction mechanism. (b) Sketch the energy…

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Q: Which is the product of the reactuon sequence? P(Ph n-BuLI CH,CH,CH,Br OCH CH2CH он CH,CH2CH…

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Q: give the mechanism of the following reactions and explain why any selectivities occur.

A: Given reaction is hydration reaction.

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.