H;C-H2C + Ph;P=CH-CH3

Q: 1. O3 g. 2. DMS for h. Na NH3 1. mCPBA 1. 2. H30* j. Cl2

A: Organic reaction mechanisms:

Q: Add curved arrows to show how carbocation A is converted tocarbocation B. Label each new σ bond…

A: Given:

Q: Draw the major product(s) for reaction of methyl pentanoate with: (2) Me2CHCH2CH2OH, H3O*

A: Transesterification: The process of exchanging an alkyl group (R) of an ester with the alkyl group…

Q: Determine the mechanism of nucleophilic substitution for attached reaction anddraw the products,…

A: INTRODUCTION: SN1 reaction is a two step reaction in which first carbocation is formed that acts as…

Q: Draw a stepwise mechanism that shows how all three alcohols areformed from the bicyclic alkene

A: Hydration of alkenes is one of the methods used for the formation of alcohol. The general steps…

Q: Show how to convert propene to this compound , using any inorganic reagents as necessary. Q.)…

A: The structure of propene is represented as follows:

Q: ccording to Zaitsev's rule, the major product of an elimination is the, substituted alkene. O most D…

A:

Q: Draw all stereoisomers formed in attached reaction.

A: This reaction is addition of halogen and water molecule on alkene. First chlorine is added to alkene…

Q: Rank the following compounds from lowest to highest heat of hydrogenation:

A: Given compounds:

Q: f) CH3 Raney Ni /H2 g) CH2CN 1. LAH/ ether. - NH-C-CH3 h) 2. H20 ahot meing

A: In the presence of a reducing agent like NaBH3CN the iminium will be reduced to give a new amine.

Q: t-BUOK -> A is the reacich SN1,SN2 ET or E2 and wnat is the Br majar product. er EtONa

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Q: Но CH-CH2 CH2

A:

Q: H2O, H* What is the major product?

A: Acidic water helps in nucleophilic addition reaction, which gets attack at double bond.

Q: Complete the following reaction by adding the missing reagents. OH CH3 ? ? ? CH3 CH3 ?

A:

Q: (a) HE H -H H₂N² Give TUPAC Name (b) Corive mechanism with Curved arrowsg th-el-

A: According to IUPAC nomenclature  an organic compound is named by identifying molecule's longest…

Q: HNO3 H₂SO4 er nitration reaction, the nitro substituent in the product will be located on carbon…

A: In nitration reaction, the -NO2 substituent is attached to a carbon atom depending upon the ortho,…

Q: 1. LIAIH,, ether major product 2 H,0°

A: We have given the organic reaction and we have to find the major product of the reaction.

Q: Complete the following reactions by providing the proper substitution AND the proper elimination…

A:

Q: Draw the complete arrow pushing mechanism for the base-catalyzed keto/en the following compound.…

A: The chemical equilibrium between ketonic and aldehydic form of same substance which get formed due…

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

A:

Q: Classify the following substituents as activators and deactivators

A: The groups which increase the electron density of the benzene ring are activators. The groups which…

Q: Provide a plausible arrow pushing mechanism for the reaction below. CI 2 eq H20 +

A:

Q: t-BUOK major product? DMSO

A:

Q: What is more stable acetate (CH3COO-) or ethoxide (CH3CH2O-)? In three words or less explain your…

A: Stability of anion: Primary carbanion is more stable than secondary and tertiary carbanions due to…

Q: CN Conc. HNO, / ACOH CH3 2- ? 3-

A: The question is based on the concept of organic reactions.   we have to identify the Product formed…

Q: Show how to convert propene to this compound , using any inorganic reagents as necessary. Q.)…

A: Hydroboration-oxidation reaction is the addition of borane followed by oxidation.

Q: Range order from lowest to highest leaving group TosO- OH-  I-  F-

A: order from lowest to highest leaving group:

Q: What compound is needed to convert styrene (C6H5CH=CH2) to eachproduct using a Heck reaction?

A: A coupling reaction where vinyl halides or aryl halides is coupled with an alkene is known as Heck…

Q: Vhat is the major product from the following reaction?

A: Since we know that  CH4MgBr Known as Grignard   reagents  and are used to reduce aldehyde , ketone ,…

Q: What type of carbocation is shown? (+)

A:

Q: Classify each substituent as electron donating or electron withdrawing.

A: Electron donating group: The group that increases the electron density on the ring. Electron density…

Q: Draw a complete arrow pushing mechanism that explains the following: Br NBS hv Br

A: N-bromosuccinimide (NBS) is used as allylic brominating reagent. 3,3-dimethylcyclohexene on…

Q: Draw the following compound on your separate sheet. (1S,2S)-5-(2methylepoxy)cyclopent-2-enol

A: Given name, (1S,2S)- 5- (2 methylepoxy)cyclopent-2-enol

Q: Draw all stereoisomers formed in attached reaction.

A: Ketones are the organic compounds which contain the -CO- group. On the reduction of ketones,…

Q: Can you please help me solve all parts of this question? (4 a, b, c, d, e, and f)

A: Since we are entitled to answer up to 3 sub-parts, we’ll answer the first 3. Kindly resubmit the…

Q: 1. reactivity towards nucleophilic acyl substitution CI HO, RANKING:

A: Nucleophile are those species which attacks on electron deficient species. In carboxylic acid and…

Q: ca/Fech major product CH + CH;CI- ACl3 Alc3

A: " Since you have posted a question with multiple sub-parts, we will solve first three sub-parts for…

Q: Draw all products, including stereoisomers, in attached reaction.

A: The given reaction is reaction of a 2-bromopentyl cyclohexane reaction with NaOCH3, and the…

Q: Arvange the folloming alfkenes n the ader of stability A) B) c) D)

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Q: Part A Complete the following reaction by filling in the necessary reagents. HyC- N.

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Q: use an organic reagents no longer than tw or three carbons or benzene to synthesis this compond

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Q: H3C-C-0-Ĉ-CH3 A FeBr3 + Br2 B (Para Product only) AICI3

A: We have given the organic reaction and we have to find the major product of the reaction.

Q: Complete the curved-arrow mechanism for the scheme below by adding any missing atoms, bonds,…

A:

Q: Draw the products formed when attached compound is treated with HNO3 and H2SO4. State whether the…

A:

Q: Draw all stereoisomers formed in attached reaction.

A: In the above reaction, the reactant is tetrahydo-2H-Pyran-2,4-diol

Q: Draw stepwise mechanisms illustrating how each product is formed.

A: The stepwise mechanism for the given reaction can be illustrated as follows,

Q: What type of carbocation is shown?

A: As we can clearly see that the positive charge (cation) containing carbon is attached to two carbon…

Q: An acetal can be hydrolyzed by treatment with aqueous acid. For the reaction below: H* catalyst H2O

A:

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.