What is the final product of the following synthesis? Н2 i. OsO4 Ni2B (P-2) ii. NaHSO4 HO Н Ш ОТ ФII OIV 2-Butyne CH3 ОН I Н CH3 CH3 НО Е Н НО H CH3 C Hig НО. CH3 Н HOH CH3 Final Product Н. НО CH3 ОН IV H CH3

Q: Complete these nucleophilic substitution reactions. In each reaction, show all electron pairs on…

A: These nucleophilic substitution reaction has to be completed. All electron pairs on both the…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. 1. Hg(CI)2, H2O 2. NaBH4, NaOH

A: Oxymercuration reaction: Hydration of alkene proceeds by an electrophilic addition reaction…

Q: Balance the following redox reaction, Br₂+ (Be sure to enter your answers as the smallest integers…

A: A redox reaction is balanced by balancing the mass and charge. Hence the number of atoms of all the…

Q: Explain why these alkyl halides form carbocations at different rates. Your answer should use some…

A: Both the carbocations formed in the chemical reaction of alkyl halides are tertiary carbocations.…

Q: How Elimination reactions can be used ?

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Q: Select the structure of the major product in the following reaction. CH;COOOH

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Q: Complete the synthesis. Show all major intermediates. ~

A: PCC oxidises primary alcohol to aldehyde and secondary alcohol to ketone.Hydroboration-oxidation…

Q: What are the steps and reagents used?

A: Applying concept of organic synthesis and reagent.

Q: What is a protecting group in a multi synthesis reaction in organic chemistry

A: Protecting groups are used in synthesis to temporarily mask the characteristic chemistry of a…

Q: Draw the arrows needed to finish the reaction below

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Q: Which is an acetal fundional grp?

A: Functional group It is an atom or group of atoms that are responsible for the characteristic…

Q: Show how the reactant can be converted to the product in two steps.

A: Cope Rearrangement Reaction: This reaction occurs under thermal condition in which 1,5-diene is…

Q: Draw the most stable resonance form for the intermediate in the following electrophilic substitution…

A: Given : structure of reactant and product.  It is a electrophilic substitution reaction.

Q: A chemistry student weighs out 0.182 g of sulfurous acid (H₂SO3), a diprotic acid, into a 250. mL…

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Q: HO MeoH

A: If the alkene reacts with the alcohols like methanol in presence of acid produced alkoxy substituted…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. 1. B2H6, THF 2. H₂O2, NaOH o

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Q: Brz Br- -Br

A: This reaction occurs through aromatic electrophilic substitution reaction. Both bromine rings are…

Q: complete this reaction

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Q: Draw the major product of the reaction. OH NaH H2 NaBr + C6H100 DMF Br

A: The chemical reaction given is

Q: 8) Show how the following conversions might be accomplished, including all reagents and…

A: The chemical reaction in which an alkyl magnesium halide reacts with carbonyl compound followed by…

Q: Acetal product formation requires an acid catalyst in the second step, but NOT in the first step.…

A: We have to predict whether given Statement is true or not.

Q: Provide the reagents to complete the synthesis. Upload your reagents and synthetic intermediates…

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Q: What is the conjugated base of this equation?

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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.