Please explain and draw the step by step mechanism of oxidation of alkynes with kmno4 and h2o/neutral on an internal alkyne.

Q: You have learned two ways to make an alkyl benzene: Friedel–Craftsalkylation, and Friedel–Crafts…

A: Alkyl benzenes are the substituted benzene in which substituent is an alkyl group. Benzene undergoes…

Q: what is the mechanism for a terminal alkyne hydroboration oxidation. the mcmurry book states this…

A: We know that  the hydroboration–oxidation reaction is a two-step hydration reaction that converts an…

Q: (Product) + Soz Mechanism of the reaction

A: The reaction of ethanol with thionyl chloride in the presence of a base like a pyridine will result…

Q: Show the full curved arrow mechanism for the following reaction, clearly showing how the indicated…

A: The first step of the reaction involved the elimination of Br- (bromide) ion to generate a 2o…

Q: Reaction of with CH3CH₂COOH forms CH3CH2CH2OH OLIAIH4 HCI KMnO4 O CH3NH2 NaBH4 as a product.

A: -> Reactant is CH3CH2COOH . -> Product is CH3CH2CH2OH .

Q: Indicate the appropriate reagent(s), conditions, and additional organic starting materials (if…

A: In the given reaction, the reactant is methylbenzene and the product formed is benzoic acid.

Q: (SYN) Hydroboration-oxidation can be carried out with deuterated forms of the reagents and solvent.…

A: Hydroboration oxidation is a reaction in which water or D2O attacks on the carbon which has more…

Q: How can you distinguish in a SNAr reaction whether it will occur according to an additionelimination…

A: The addition-elimination reaction or elimination-addition reaction comes in the category of SNAr…

Q: Give the major product(s) of the following reaction.

A: The major product of the given reaction can be shown below

Q: Show the complete mechanism using Curved Arrow Formalism for the reaction of the compound shown…

A: INTRODUCTION: p-chlorobenzaldehyde reacts with EtOH and HCl to give an acetal.

Q: Provide the major organic product of the following reactions. Show the complete arrow pushing…

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Q: (e) When treated with base, the compound shown below cyclizes. Show the structure and relative…

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Q: Provide an arrow pushing mechanism for the following reaction. Make sure to include initiation,…

A: It is a radical addition reaction. It is first explained by Karasch. It is also known as Karasch…

Q: Treatment of but-2-yne with NCS affords an interesting molecule with two methoxy groups and

A: N-chloro succinimide is abbrivated as NCS .  In presence of polar solvent Chloronium ion is…

Q: A student wanted to prepare (1-Ethylpropoxy)cyclopentane by heating cyclopentanol and pentan-3-ol…

A: The given structure is represented as follows:

Q: please show and explain the mechanism of the Formation of epoxide by reaction of an alkene with a…

A: Peroxy acids are generally unstable in nature but meta-chloroperoxybenzoic acid is an exception. It…

Q: From the cope elimination,indentify the major product for this rection and propose the mechanism to…

A: Cope elemination :-          In this reaction tertiary amine oxide undergo the elimination of a…

Q: H3C

A: Detail synthetic pathway is given below

Q: Explain mechanism for the addition of two equivalents of HX to an alkyne ?

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Q: Provide the complete mechanism using Curved Arrow Formalism for the reaction of potassium…

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Q: For the following reaction, draw the correct product that you would expect to form under Robinson…

A: Given - Product = ?

Q: of indiante which is the main product. Justify your answer. 6) present the possible mechanism for…

A: To answer: Indicate which is the main product. Justify your answer. Present the possible mechanism…

Q: lodine monochloride (ICI) is a mixed halogen that adds to an alkene via the same mechanism by which…

A: Iodine is less electronegative than chlorine. So the splitting of the I-Cl bond shall result into…

Q: Show by series of reactions how n-bromobutane can be synthesized from: a. butane b. butyne

A: We have to show by series of reactions how n-bromobutane can be synthesized from: a. butane b.…

Q: Draw the major organic product of the reaction shown.

A: The reaction proceeds in two steps.  In the first step, a proton is added to the hydroxyl group to…

Q: Illustrate the mechanism of forming alkynes from a 1,2-dihalide and a vinyli halide. Show…

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Q: OTs - (strong base) В Doubling [B] doubles rate of rxn.

A: The reaction involves a carbocation intermediate and is commonly seen in reactions of secondary or…

Q: Complete the following reaction by drawing the structure of the major product(s) expected.

A: The hydration reaction is the electrophilic substitution reaction. The hydration reaction of alkene…

Q: Provide a reasonable mechanism that provides the major product for the reaction scheme provided…

A: The reaction given is,

Q: different reactions with specific conditions given (i.e., reagent and solvent). -Please include…

A: Given; The starting material is propene. , CH3- CH2=CH2 Let's try to make an ether from propene. The…

Q: HO HO,

A:

Q: -- А he main product of the following reagen with compound A.

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Q: HO H2SO4 H2O, heat

A: This reaction proceed through E1 mechanism And the product of this reaction is

Q: Propose a mechanism for the α,β-elimination reaction.

A: A mechanism for the α,β-elimination reaction has to be given

Q: Draw the organic product(s) of reaction of the alkyne above with H3O+ in the presence of HgSO4.

A: The given compound is – 3, 8-dimethyldec-5-yne.

Q: Provide the reagents and products for the nitration of toulene and explain why. Draw a detailed…

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Q: Br2 and light CC14 solvent

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Q: Draw an alkyl bromide with proper stereochemistry that can be used to synthesize the given alkene as…

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Q: Br2 H20 CH3CH,CH,CCH,Br CH,CH,CH,C=CH

A: The mechanism of the following reaction is as follows:

Q: Draw the structure of compounds (E-H) from the following cycloaddition reactions.

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Q: Indane can undergo free-radical chlorination at any of the alkyl positions onthe aliphatic ring.…

A: Indane is an organic compound which two part, one part is an aromatic ring and other part of the…

Q: Treatment of but-2-yne with NCS affords an interesting molecule with two methoxy groups and two…

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Q: please explain the mechanism of ring opening of an epoxide by reaction with nucleophile under acidic…

A: The reactions of Epoxides with strong nucleophiles requires a strong driving force that helps in the…

Q: Add missing reagent(s) while also showing stereochemistry of the product of the second reaction.

A: In this question we have to complete the given organic reaction.

Q: Part A: Describe the mechanism for dihydroxylation of an alkene through the use of a peroxide…

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Q: Acid-catalyzed dehydration of cyclobutylmethanol proceeds via an El mechanism and gives two alkenes.…

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Q: the complete mechanism for the tautomerization of 3-butanone under...

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Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.