Consider a reaction where cis-hex-3-ene is treated with Oso followed by NaHSO₂/H₂O.

Q: Draw the structure of the major organic product of the reaction. CH3 CI 1. LIAIH4, ether 2. H30+ •…

A: Lithium aluminum hydride (LiAlH4) is a versatile reducing reagent, that reduces the acid chloride…

Q: Propyne is reacted with NaNH2. The major organic product of this reaction is then reacted with…

A: We can write the IUPAC name of alkyne using following rules Identify parent chain ( chain with…

Q: 1. Provide the reagents or product for the following chemical reactions. When necessary, show…

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

Q: Draw a structural formula for the major product of the reaction shown. H3C Cl2 H3C H20 • Show…

A:

Q: w the structure of the product, showing S 3-methylcylopentene

A:

Q: Show how to prepare each alkyne from the given starting material. In part (c), D indicates…

A: Given reaction is,

Q: Draw the products formed when both cis- and trans-but-2-ene are treated with OsO4, followed by…

A: The objective of the question is to predict the products formed when cis and trans  is reacted with…

Q: Draw the major organic product of the following sequence of reactions. Show stereochemistry in the…

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Q: 20. C2 CH;OH 21. (1) O3 (2) (CH3)2S 22. CH;OH H,PO4

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Q: ho NBS hv

A: Given reaction is photolytic bromination reaction.NBS is N-bromosuccinimide.This is allylic…

Q: Using cis- and trans-hex-3-ene, demonstrate that the addition of HCl is not a stereospecic reaction.…

A: Stereospecific reactions are reactions in which reactants differ only in their configuration are…

Q: If the reaction of an alcohol with PB13 follows an SN2 mechanism, what is the stereochemistry of the…

A: SN2 Mechanism: It is an substitution reaction in which nucleophile attacks on organic compound with…

Q: What could be the product of this alkene as it reacts with reagent KMnO4?

A: KMnO4 is a strong oxidising agent  If alkene is treated with KMnO4 ,  it is oxidised into…

Q: Draw the product formed when (CH3)2CHOH is treated with following reagent. TsCl, pyridine

A: Given, TsCl, pyridine

Q: Draw the major organic product(s) of the following reactions including stereochemistry when it is…

A: Alkyne gives a hydration reaction in the presence of sulfuric acid and a mercuric acid catalyst to…

Q: NaH CH;CH2I i. HO CH2CH3

A:

Q: Complete the reaction by writing the main product or products that lead to the indicated product. If…

A: In the first step of this reaction, aldehyde react with amonia form imine compound,this reaction…

Q: Give the product of the following reaction, showing stereochemistry. NaCI CH,OH

A: epoxide are electrophilic in nature so it undergo nucleophilic substitution reaction

Q: Draw the major organic product of the reaction. Indicate the stereochemistry via wedge/dash bonds,…

A: The product obtained afer nucleophilic substitution of primary alkyl bromide given is as shown…

Q: H2SO4, H2O DMSO, (COCI)2 EtgN OH

A: The reactions given are,

Q: The following two reactions undergo E2 elimination. Reaction (a) gives two products while reaction…

A: The question is based on organic reactions.We need to identify the product and explain its…

Q: Compound A reacts with one equivalent of H₂ in the presence of a catalyst to give methylcyclohexane.…

A: Given,Compound A reacts with one equivalent of H2Compound A can be formed upon treatment of…

Q: gnoring stereochemistry, draw the alkylborane formed from the addition of one equivalent of BH3 to…

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Q: The main product of the reduction of 3-ethyl-2-pentanone, in the presence of LIAIH4 as catalyst, is:…

A: Given,The main product of the reduction of 3-ethyl-2-pentanone in the presence of  LiAlH4 is:

Q: When 2-Methylcyclohexane-1,3-dione was treated with 3-buten-2-one in the presence of EtONa (base),…

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

Q: Treatment of (2R, 3R)-2,2-epoxy-3-methylpentane with aqueous acid results in a ring-opening…

A: Draw the product and intermediates of the given organic reaction.

Q: Show how to prepare each alkyne from the given starting material. In part (c), D indicates…

A: Bromination of alkene gives dibromo alkane.

Q: МСРВА Alkenes are oxidized to give epoxides on treatment with a peroxyacid, RCO;H, such as…

A: Note: Epoxidation of olefins using mCPBA. For mechanism see below. Here olefin is act nucleophile…

Q: Draw the major organic product of the reaction conditions. Show stereochemistry in your structure.…

A: The use of osmium tetroxide is a useful reagent for dihydroxylation of alkenes.Produces syn addition…

Q: H2 (g) Pt/C catalyst

A: Given,  Reactant = 4-Methyl-2-pentene  Reagent = H2 (g), Pt/C catalyst  Product of the reaction = ?

Q: Account for the regioselectivity and stereoselectivity observed when this compound is treated with…

A: Addition of HX follows Markovnikov's addition, i.e., when HX is added to an unsymmetrical alkene,…

Q: Fill in the missing reactant, reagent and products. Indicate stereochemistry if necessary. Unless…

A:

Q: conjugated ring with alcohol reacts with I2, NaHCO3 with CH2Cl2 and H2O. What will be the product?

A: The reaction scenario described involves the interaction of a conjugated ring containing an alcohol…

Q: Draw one of the major products from this reaction. Use wedge and dash bonds to indicate relative…

A: The metal zinc (Zn) is inserted in the carbon-iodine (C-I) bond of diiodomethane (CH2I2) to form the…

Q: Show how to bring about each conversion in good yield. In addition to the given starting material,…

A: We can obtain β-azidoalcohol by stereoselective ring opening of the azide ion.

Q: H,NNH, КОН CH3 calor

A:

Q: Account for the regioselectivity and stereoselectivity observed when 1-methylcyclopentene is treated…

A: For bromine and water addition, the hydroxyl group will bind to the most substituted carbon (the one…

Q: Draw the product formed when (CH3)2CHOH is treated with following reagent. POCl3, pyridine

A: Alcohol are the type of organic molecules that contain OH functional groups. The reaction given…

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.