Draw the mechanism for oxymercuration-demercuration  with the following alkene. 2-methyl-1-butene

Q: Draw mechanism arrows and then predict the major products and stereochemistry. Also include the…

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Q: Hg2+ Но c=CH2 H3C H3C-C=C-H H30

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Q: Once treated with HBr, which alkene is the most likely to undergo a carbocation rearrangement after…

A: Given that : We have to identify which of the following alkene is the most likely to undergo a…

Q: In the following reaction the leaving group is: I- + CH3O-COCH3 --> CH3I + CH3CO2-

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Q: H3C H H „CH3 NaOCH3 Br

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Q: The major product that would form from the presented reaction scheme is? CH3 H2/Pd NO2

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Q: Determine the mechanism and draw the products of attached reaction. Include the stereochemistry at…

A: SN1  : It is the uni-molecular Nucleophilic Substitution. The first step of the mechanism is the…

Q: If a mixture of products is expected, the more stable alkene is the major product. Recall that the…

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Q: Name the following alkene and draw the product of the reaction with KMnO4.

A: The hydrocarbons in which two of the carbon atoms are bonded to each other by a double bond are…

Q: Draw the mechanism for oxymercuration-demurcuration  with the following alkene. 2-methyl-1-butene

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Q: Draw the products of attached reaction, and indicate the stereochemistry where appropriate.

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Q: Decide on the mechanism for the following substitution, and then pick the solvent that affords the…

A: In both solvent’s cases, we will proceed the reaction through an intermediate stage and look for…

Q: show the arrows of this reaction mechanism,

A: The arrows of this reaction mechanism can be shown below The major product should show a…

Q: Show the step-wise mechanism of the following radical reaction, indicate major product if one is…

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Q: Please explain and draw the step by step mechanism of oxidation of alkynes with kmno4 and…

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Q: Draw the product or products of the reaction. Include charges where appropriate. Draw the…

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Q: 1. NaH Cycliza O°H

A: Given transformation is,

Q: Draw the four resonance forms of the allylic carbocation intermediates when the alkene below reacts…

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Q: n the presence of light or heat, diazomethane (CH,N2) creates a carbene, which then adds to an…

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Q: Draw the product for the following alkene addition (hydrogenation) reaction.

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Q: Draw the mechanism for the following reaction and account for the relative stereochemistry. MeO₂C…

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Q: Which of these reactions is a syn addition? Addition of C12 across an alkene o Ozonolysis Opening an…

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Q: The major product that would form from the presented reaction scheme is? CH3 H2/Pd NO2 O=U

A: The solution of above reaction is-

Q: Draw the product of attached asymmetric epoxidation reaction.

A: A three membered ring that contains two atoms of carbon and one atom of oxygen is called as epoxide.…

Q: Draw the mechanism for the formation of the epoxide of cyclopentene with first Br2/H2O followed by…

A: We have to predict the mechanism for the formation of epoxide of cyclopentene.

Q: Label the following alkenes from most stable, moderate and least stable.

A: Various alkene is given  Stability Order = ?

Q: Decide on the mechanism for the following substitution, and then pick the solvent that affords the…

A: SN1 reaction It is a two step nucleophilic substitution reaction in alkyl halides. The rate is…

Q: Draw the complete mechanism for this reaction. p-CH3- CgH4– SO;H + H3C-OH

A: The organic conversion helps in the conversion of one organic compound into other compounds. This is…

Q: monobromination

A: Br2 give Radical substitution reaction in the presence of sunlight. Inwhich Br2 broken in Br•…

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

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Q: This is the general mechanism of nucleophilic addition of aldehydes and ketones. Nu: Nu- H-Nu…

A: Aldehyde and ketone undergo nucleophilic addition reaction. Aldehyde gives primary or secondary…

Q: CH3 H2/Pd NO2 O=U

A: Here reduction will occur.

Q: Complete the mechanism of hydration of alkene below. Please follow curved arrows to predict the…

A: Answer:- The hydration of alkene gives the corresponding alcohol according to Markovnikov rule which…

Q: Which of the following additions to alkenes occur(s) specifically in an anti fashion A)…

A: Solution: Hydroboration-oxidation: in this reaction water molecule adds to alkene in anti…

Q: Draw the major intermediate and product of the reaction between (2E)-4-methylhex-2-ene and Br, in…

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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 a detailed mechanism for the addition of H20 to 2-methyl-2-pentene in the presence of H2SO4.…

A: The structure of  2-methyl-2-pentene is as shown below In reaction with H2SO4, the proton from the…

Q: Draw

A: Oxymercuration-demercuration reaction of 1-octene yields an alcohol. Detailed mechanism is shown in…

Q: Complete the following transesterification reaction

A: Transesterification is the reaction of the exchange of organic groups between ester and alcohol to…

Q: HO OH OH HCI H. H.

A: A carbocation is an electron-deficient species that has a positively charged carbon. In this…

Q: NaH + CI- NaCl DMF

A: NaH is a strong base. ,so it will produce H- ,Which will try to abstract acidic H of alcohol are as…

Q: Draw the products (including stereoisomers) formed when (S)-2,4-dimethylhex-2-ene is treated with…

A: Anti Markonikov rule  Alkenes on reaction with HBr in the presence of peroxide forms an addition…

Q: Show the mechanism to form 2-chloro-2-methylpentane, but not 2-chloro-4-methylpentane. H-CI H -CI

A: The reaction given is,

Q: Draw the mechanism for the reaction of 1-Methylcyclohexene with hydrogen bromide.

A: Reaction of HBr with 1-Methylcyclohexene is the type of addition reaction. Addition of HBr follows…

Q: Choose the mechanism that forms the main product of the following reaction. Er ONa CH3CHOH calor

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Q: Draw the mechanism for the reaction of cyclohexene with HCl.

A: The cyclohexene reacts with HCl via electrophilic addition.

Q: Write down all possible alkene products from the following Elemination reaction (no mechanism is…

A: Alkenes are the organic compounds which contains at least one double bond present in it. These can…

Q: Add any remaining curved arrow(s) to complete step 4 of the mechanism. Modify the given drawing of…

A: The reaction mechanism step given is,

Q: What is the intermediate component formed during ozonolysis of an alkene? an ozonide O osmate O…

A: In this question, we will see the intermediate during the ozonolysis of the alkene compound.  You…

Q: K* -OCH2CH3 Br-

A: Strong base ---------> E2 elimination Smaller base --------->Greater substituted alkene