(1)RCO,H, CH,Cl2 (2)H;O*

Q: What is the major product of the following reaction || IV I & III ۵۰۰ III صد IN

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Q: NaOEt ELOH

A: The major product of the given reaction is given bleow : Above reaction is an example of michael…

Q: C15T09Q5917 Give the major product of the following reaction. NaOCH3 F- NO, heat

A: Aryl halide does not react in nucleophilic substitution reaction, but if electron withdrawing groups…

Q: Provide the major organic product of the following reaction. H3CH2C CH2CH3 HNO3, H2SO4

A: The given reaction is electrophilic aromatic substitution reaction. In this reaction nitration is…

Q: Draw reaction mechanisms with all reactants, arrows, intermediates, and products. Your mechanism…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Draw the principal organic product of the following reaction. OEt OEt 1. NaOEt 2. H,C- 1. NaOEt — Br…

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Q: Predict the major product for the following reaction. CN heat Modify the given structure of the…

A: The first reaction is hydrolysis of nitrile which gives carboxylic acid as a product. The second…

Q: 애 X™ + HCCl3 +

A: The objective is to determine the reaction product. The reactants include; isopropyl alcohol…

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

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Q: Br NaO₂ CCH3 CH3CO₂H low temp.

A: Sodium acetate can be used to form an ester with an alkyl halide.

Q: Match the reactant with the product of its reaction with HClO4. Leave blank if there is no…

A: Using double displacement reaction concept and oxidising nature of HClO4 we can determine the…

Q: a) CH;CH,ONa H3CO ethanol 5) 1) LIAIH4 2) H20 H3CH2CO

A: Products produced from above reactants

Q: EtO₂C NO₂ NH₂OAc glacial HOAC benzene/A

A: Here ammonia being basic removes the acidic proton of active methylene group .

Q: structures of the major products formed in the following reactions. Use mechanisms to justify the…

A: The given reactions are shown below.We have to draw the product of the reaction with the mechanism.

Q: a. Reagent(s) and conditions for the conversion of Compound B to Compound A. b. Reagent(s) and…

A: Conversion of one compound to another compound using reagents are ,-

Q: Provide the major organic product(s) for the following reactions. AICI, CH₂NO H₂SO4

A: In Given  reaction first reaction  is fridel craft acylation reaction

Q: Provide a stepwise synthesis to carry out the following conversion. CHÍNH,

A: In this organic reaction several multiple steps are involved.The following steps are involved.

Q: Provide the IUPAC name of the product formed from the following reaction. If no reaction is…

A: The reactant is a ketone. The reagent is . The reagent is called Tollen's reagent.

Q: Please provide the steps that each carbonation will undergo to form a carbonation that is more…

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Q: Indicate the major organic product from the reaction shown. HO OH 1. NABH4 HQ: HO 2. Нао HO,

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Q: Give the major product of the following reaction. H2NNH2, NaOH heat

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Q: Indicate the major organic product from the reaction shown. Culi Br

A: The answer is as follows:

Q: Provide the curved-arrow mechanism to account for the following nucleophilic addition reaction. H20…

A: Hydrolysis of amine to nitrile is nucleophilic addition reaction. And mechanism for this reaction…

Q: Draw the major organic product for the reaction shown. HO. O: HCI (cal.)

A: We have to predict the major product.

Q: Provide the major organic product in the reaction shown below. H;O", A O:

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Q: Provide the major organic product of the following reaction. CH3 HNO3, H₂SO4, A

A: The given reaction is electrophilic aromatic substitution reaction. In this reaction nitration is…

Q: Give the major product of the following reaction. 1) 03 2) Zn, H20

A:

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.