Draw the major product for the reaction, showing the stereochemistry by using wedge bonds. The product will be racemic but show only one enantiomer. Clearly show stereochemistry by drawing one wedged, one dashed and two in-plane bonds per stereocenter. Remember that a hydrogen atom on a chirality center must be shown explicitly and with a wedge or dashed bond. Select Draw Rings More Erase Cl2 CH3CH2OH

Q: Draw one of the two enantiomers of the major product from this reaction. Use a dash or wedge bond to…

A: First of all Br2 reacts with alkene and forms cyclobromonium ion. This bromonium ion can be broken…

Q: The reaction shown forms two major substitution products. Draw both products and write a mechanism…

A: The compound given is tertiary alkyl halide which reacts with Methanol by Unimolecular Nucleophilic…

Q: Draw the major products of the SN1 reaction shown below. Use a dash or wedge bond to indicate…

A: In SN1 mechanism, there is formation of Carbocation intermediate.In SN1, a racemic mixture form.

Q: H3C HO HO OH OH OH OCH3 1. (COCI)2, DMSO 2. NEt3 CrO3 H₂SO4 H₂O (excess of all reagents) DMP 1…

A:

Q: Draw the major product of this reaction. Include stereochemistry if applicable. Use a dash or wedge…

A: The reactions in which  an atom or a group of atoms are replaced  by another atom or group of atoms…

Q: Highlight in red the higher priority substituent on each end of the blue double bond. Im

A: Given is organic compound.Given compound is alkene.The priority of groups is assigned according to…

Q: Label the reactive features of the following set of reactants, select the most reactive feature,…

A:

Q: Br₂

A: This is bromination reaction of an alkene. The reaction proceeds through formation of a bridged…

Q: Be sure to answer all parts. Draw the products formed, disregarding stereoisomers, when the…

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

Q: Draw the structure of the major product. If the answer for the

A: 1. Addition of Br2 /H2O : it is a trans/anti addition product formed is bromohydrin , cyclic…

Q: None

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Q: For the dehydrohalogenation (E2) reaction, draw the Zaitsev product, showing the stereochemistry…

A: The given reactant is (2R,3R)-2-iodo-3-methylpentane. It is an undergoing E2 elimination reaction…

Q: Use the starting material and any other reagents/solvents of your choice to synthesize the molecule…

A: In this question, we will synthesized the final organic product from the starting material alkene.…

Q: W Draw the structures for (Z)-3-methylhex-3-ene and the two major organic products for its reaction…

A: HBr addition to alkene gives an alkyl halide according to Markoniokov's rule.

Q: What is the major final product of the following reaction sequence? Only ane enantiomer of the…

A: The possible product has to shown

Q: structures are fragments of major product of dehydration reaction of 2-methylbutan-2-ol.  need to…

A: The alcohol functional group is identified as by the presence of the -OH unit in the molecular…

Q: expected major product for the indicated reaction If the answer for the product is a mixture of…

A: 1. Here, SN2 reaction gives cyano compound as DMSO is a polar aprotic solvent.  2. Here, SN2…

Q: OCH3 Draw Major Product + Draw Minor Product

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Q: 9. Upon treatment of strong base 4 undergoes an E2 elimination. Answer the following questions about…

A: Step 1: Step 2: Step 3:Step 4:

Q: 10. When cyclohexane 5 is treated with a strong base it undergoes an E2 elimination. Answer the…

A: Step 1: Step 2: Step 3: Step 4:

Q: The 1,2-dibromide is synthesized from an alkene starting material. Draw the alkene starting…

A: The characteristic reaction of alkene is electrophilic addition reaction. The addition of Br2 takes…

Q: Draw an alkyl chloride that would produce ONLY the following alkene in an E2 elimination. Use a dash…

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Q: 0 ་ Draw the major organic product(s) of the following reaction. Br DMF + KCN You do not have to…

A:

Q: d) e) H OCH 3 HN -NH NaBH4 CH3OH H₂ Pt/C Pd/C H₂ 1 enantiomer (1 chiral compound) 1:1 mix of…

A: NaBH4 acts as mild reducing agent and it reduces carbonyl group but it cannot reduce ester group.…

Q: Fill in the major products to complete the transformations. Be sure to pay careful attention to…

A: It is based on the concept of reactivity of alkene. Here we are required to find the product of the…

Q: 6. Draw the products for each of the following reactions. Using wedges and dashes, indicate the…

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Q: Circle all of the compounds below that would react with NaBH AND produce a pair of enantiomers.…

A: ->NaBH4 is reducing agent which can reduce carbonyl compounds to alcohol but it can not reduce…

Q: 2. For the following transformations draw the product in the box below. Draw only one stereoisomer…

A: Concept used is-Hydroboration oxidation reaction and regioselectivityOzonolysis reaction in the…

Q: Draw one enantiomer of the major product of the Diels-Alder reaction shown. Use wedged and hatched…

A: To find the product formed by Diels Alder reaction. Diels Alder reaction is a [4+2] cycloaddition…

Q: Draw one enantiomer of the major product of the following Diels–Alder reaction shown. Use wedged and…

A: Product of Diels alder reaction with proper stereochemistry and it's Enantiomer is shown in the…

Q: Is the curved arrow mechanism reasonable? yes O no Click and drag to start drawing a structure.

A: In the first question, we have to predict that given mechanism is possible or not and also have to…

Q: The 1,2‑dibromide is synthesized from an alkene starting material. Draw the alkene starting…

A: Alkenes typically react in an electrophilic addition reaction. Br2 is added in a way that causes the…

Q: H₂O Edit One of the Major Products Br + Edit. One of thMaior Products heat Draw One of the Major…

A: Given that, the reaction is:

Q: 3. For the following transformations draw the product in the box below. Draw only one stereoisomer…

A: LDA is a strong base which also sterically bulky. Thus it accepts protons from less congested…

Q: Examine the curved arrow mechanism below, and answer the question in the box. If the mechanism is…

A: During mechanism flow of electrons occur from higher electron density to lower electron densityA…

Q: Draw the products resulting from addition of a Grignard reagent to an aldehyde. Use a dash or wedge…

A: It is based on the concept of Grignard reaction.Here we are required to find the product of the…

Q: Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers.…

A: Epoxides are the three membered cyclic ring containing oxygen atom.This ring has strain so it can…

Q: Draw an alkyl halide that would undergo an SN2 reaction to yield this product under the conditions…

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Q: ← Draw the products of the two step reaction sequence shown below. Ignore inorganic byproducts. ←…

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Q: Draw the major product of the reaction shown below. Use a dash or wedge bond to indicate…

A: Electrocyclic ring-opening reactions occur when a cyclic compound undergoes ring opening under the…

Q: Provide the missing reagent or product for each reaction below. Where necessary, indicate the…

A: Given reactions are shown below.We have to give the missing reactants, reagents and the products.

Q: Given the following reaction conditions, and assuming excess Hg reagent and water, draw the two…

A:

Q: Draw the products resulting from addition of a Grignard reagent to an aldehyde. Use a dash or wedge…

A: During the Grignard reaction, initially, the nucleophilic carbon (C) atom in the Grignard reagent…

Q: Draw one enantiomer of the major product of the following Diels-Alder reaction shown. Clearly show…

A: Diels-Alder reaction: The Diels–Alder reaction is a reaction between a conjugated diene and a…

Q: Draw the major product formed in the reaction. Use wedge-and-dash bonds to show the stereochemistry…

A: We have given an unsymmetrical epoxide and a reaction of an unsymmetrical epoxide with sodium…

Q: a BH-THF Click and drag to start drawing a structure.

A: The given reaction involves the hydroboration reaction of 5-memeber cyclic alkene.The hydroboration…

Alkynes

Alkynes are organic compounds that contain at least one triple bond between carbon-carbon atoms. They are a series of unsaturated compounds with a general molecular formula, CnH2n-2.