05 Question 2 Provide the structure of the major organic product of the following reaction. NaCN H3C H3C 11 I IV Br "CN Question 3 H3C II CN ? H3C III Na H₂C IV CI

Q: НО, ОН ОН ОН CO₂Et

A: To provide the synthetic route for the iven target molecules from the iven starting materials

Q: 2. By what type of mechanism does the following aromatic substitution reaction proceed? Draw the…

A: The given reaction is an example of  nucleophilic aromatic substitution reaction. The mechanism of…

Q: Outline a synthesis of the following compound from the given starting materials. OH OH from

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Q: HO. O,N

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Q: Provide the curved-arrow mechanism to account for the following nucleophilic addition- elimination…

A: Nucleophile attacks on carbonyl carbon to produce tetrahedral intermediate. This tetrahedral…

Q: Give the product for the following reaction scheme. Br 1) Mg° 2) H₂O

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Q: Rz BH 三 ho

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Q: Write the mechanism for the following reactions. Explain detail each steps of reactions. a)…

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Q: From benzene, organic compounds with 6 carbons of less and any other inorganic compund you want.…

A: Given that : We have to synthesize the following naphthalene derivative from benzene :

Q: rovide a structure for the major product

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

Q: Give the reaction conditions which could be used to bring about the transformation shown in two…

A: Oxidation and reduction are the key steps here. These steps will result in our desired product.

Q: Provide a synthesis for of the following reactions. Show each intermediate structure between steps.…

A: Step 1: Step 2: Step 3: Step 4:

Q: provide synthesis for this reaction including all reagents and mechanisms with steps ↑

A: This can be done like this

Q: B) Benzene to N-methyl-3-phenyl propanamide Он c)

A: The synthesis of the following is:

Q: From naphtalene and any other organic or inorganic compund you want, synthesize the following…

A: Synthesis of desired product involves multiple steps. These are : sulfonation (TCP), Bucherer…

Q: 2) Provide a synthesis for the product shown below given the starting material. ОН ОН

A: By observing the starting material and the product, we can see both the reactant and product are…

Q: Predict the organic product of the reaction. Include all hydrogen atoms

A: In the presence of sulfuric acid, alkene undergoes to hydration to produce alcohol. The kinetic of…

Q: The reaction is a nucleophilic substitution, A is OH- and B is an alkyl bromide. Give the reaction…

A: The nucleophilic substitution reaction of alkyl bromide with OH- is given below

Q: шавни

A:

Q: Propose a sequence of reactions to synthesize the target compound below from the indicated starting…

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Q: Using the Malonester synthesis, write the synthesis of the following compound by showing its…

A: malonester synthesis is the chemical process in which the diethyl malonester is alkylated at the…

Q: Enamines can serve as enolate surrogates in reactions at the a-carbon. In the reaction sequence, the…

A: At first carbonyl oxygen undergo protonation to increase the electrophilicity of carbonyl group of…

Q: Show how you would synthesize each compound from benzene, toluene, or phenol using the following…

A: The starting materials are benzene, toluene or phenol Reactions are 1. Halogenation 2. Nitration 3.…

Q: Can someone Outline a chemical reaction for the formation of the compound and explain it and detail…

A: Details explanation of above reaction is given below.

Q: Propose a synthesis for the following compound.

A: The question is based on the concept of organic reactions.   We have to convert the reactant into…

Q: سلم من في .. معه from

A: Organic transformation

Q: Show how the following compound can be synthesized from benzene.

A: Friedal Craft Alkylation: The addition of an alkyl group in the presence of Lewi acid is called…

Q: OH O,N NH2

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Q: The mechanism for this reaction involves 2 4 1 3 Br steps CH3CH₂OH Heat

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Q: OTos Ph

A: Since OTos is a strong leaving group. Hence the reagent given above arrow will attack on the…

Q: Br2, aq. NaOH NH2

A: Hoffmann bromamide reaction is a reaction where primary amines are prepared. The amine obtained will…

Q: 22) Which of the following statement(s) is (are) TRUE? a. Zaitsev's rule: If substrate is a tertiary…

A: Zaitsev's rule: If the substrate is a tertiary alkyl halide and the base is small, E2 mechanism…

Q: a. b. Br Br MeO OMe

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Q: Carbon NMR Spectrum A has peaks at & 71, 40, 19, and 12. Spectrum B has peaks at 8 72, 38, 31, 29,…

A: The solution is as follows:

Q: оссH2CH3

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Q: Draw the structure of the major product for each of the below reactions. If a reactions gives a…

A: Step 1: NaNH2 is a very strong base. NH2- abstracts proton from the terminal methyl group of 1 to…

Diol

In chemistry there are so many chemical compounds that have a hydroxyl group but a chemical compound having two hydroxyl groups (-OH) is termed as a diol. It also implies the presence of two alcohols whereas polyols contain two or more than two hydroxyl groups (-OH). Glycol or 1,2-diol is an aliphatic diol that has two alcohol groups on adjacent carbon atoms. In industries, the most commonly used diol is ethylene glycol.