OH CH3 H* H;CH,C ´OH

Q: Draw the structure of the major product of  Benzene + HNO3 in H2SO4

A: Benzene undergo electrophilic substitution reaction and in the reaction, a hydrogen atom of benzene…

Q: Draw a stepwise mechanism for the conversion of heptane-2,6-dione to 3-methylcyclohex-2-enone with…

A: First, the general equation is as follows,

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: Draw a stepwise mechanism for the conversion of hex-5-en-1-ol to the cyclic ether A.

A: H2SO4- H2SO4 is sulphuric acid This is strong acid. An acid completely dissociate in aqueous…

Q: CH3 -CH3 KMN04 (warm, conc.) CH3 H

A: Oxidation of 3-methyl Hex-3-ene:

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: Но CH-CH2 CH2

A:

Q: Wellbutrin (1) is an antidepressant used to treat major depressive disorder. Add the missing…

A: The answer to the following question is-

Q: Write IUPAC name of the major product formed as a result of the reaction indicated CH3 H* + H,0 ?

A:

Q: Select the structure of the major product in the following reaction. CH;COOOH

A:

Q: What alkene can be used to prepare each alcohol as the exclusive product of a two-step…

A:

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

A:

Q: Draw the organic product of the following reaction. H2SO4 / H20 H3C CH2-C=CH CH H9SO4 ČH3

A: The product of the reaction has to be drawn.

Q: Draw the major product of this reaction. Ignore inorganic byproducts and the alcohol side product.…

A: Substrate given in the question is an ester and the reagent given is acid The reaction is basically…

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

A:

Q: + en

A:

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: Synthesize each compound from toluene (CgH,CH3) and any other organic or inorganic reagents. a.…

A: Hey, since you are posted a question with multiple sub-parts, we will answer first three sub-parts.…

Q: H3CO. 1. NaOCH3 2. H20 OCH3

A: Any molecule or ion which are electron rich species are called nucleophile for example -NH2,-OH and…

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

A: Given

Q: Write IUPAC name of the major product formed as a result of the reaction indicated .CH3 Pd + H2 ?

A: In this given reaction,  The 1-methylcyclopent-1ene reactant is a starting material or reactant is…

Q: Complete the following Fischer esterification reaction

A: When an alcohol reacts with a carboxylic acid in the presence of an acid to form an ester is called…

Q: W X Select reagent W and Y 1 HNO3 H₂SO4 2 CH3C1₂ AICI 3 3 Cl₂, FeCl3 ) 4 503, H₂SO4 NO₂ S0₂t

A:

Q: The common name for the follouing compound Ps: a) disec -butyl-ether b) dPbutyl ether c) I-…

A:

Q: Draw the organic products formed when 4-octyne is treated with each reagent. a. H2 (excess) + Pd-C…

A: Since we only answer up to three subparts, we'll answer the first three. please resubmit the…

Q: Identify the major product. X Heat ?

A: Pericyclic reactions are those which can take place in presence of light or sunlight. These…

Q: What

A: First OH- attack on carbonyl carbon and then π bond transfer towards more electronegative atom…

Q: Write IUPAC name of the major product formed as a result of the reaction indicated CH3 H3C H* + H20

A:

Q: Show a stepwise mechanism by pushing arrows and drawing all intermediates. Draw a detailed mechanism…

A: The reaction of an alkene with water in acidic medium follows below mechanism  1) The alkene takes a…

Q: 0-

A:

Q: HO3S- -CH3 Br CH3

A: Detail mechanistic pathway is given below to carry out the conversion

Q: i. O3, ii. PPh3 CH2CI2 H

A: The mechanism is as follows:

Q: Draw the major organic product formed by reaction of 2-hexyne with the following reagent: H₂O in…

A: The starting material is 2-hexyne which is represented as: In this reaction, a molecule of water is…

Q: а) b) c) OEt

A: When aldehyde or ketone react with diol or alcohol it form acetal.

Q: Analyze the reaction below, and then provide the reagents necessary to carry out the conversion. Be…

A: The answer is given below

Q: Draw the major product of this reaction. Ignore inorganic byproducts and the alcohol side product.…

A:

Q: Consider carbonyl compounds A– E attached  below. Which compound is most reactive in nucleophilic…

A: The stability of the carbonyl compound can be determined by the electrophilic character of the…

Q: F3C² CF₂ reactive acyl Most -nucleophilic اعم least substitution H3C reactive CH3 3 to word

A: Dear student since you have asked multiple questions but according to guidelines we will solve 1st…

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

A:

Q: Provide the reagents necessary to complete the following transformation. CH, -CH3 to

A: free-radical halogenation (more substituted alkyl halide is formed) E1 elimination  acid catalyzed…

Q: H3C CH3 ito OH но. OH Но но Но

A: Hemiacetal compound is the compound fromed by the reaction of carbonyl compound and one alcohol…

Q: Write IUPAC name of the major product formed as a result of the reaction indicated CH3 H3C Ni + H2

A: The reaction given is,

Q: Draw the major organic product. H,C CH, Br H H3C CH3 H2 HC CH H3C- H H-Br H

A: HBr addition in alkene proceeds via formation of a stable carbocation. The mechanism is shown below…

Q: S O NaBH4 OLIAIH4 OBH3, THF OLIAIH(O'Bu) 3 OH

A: Organic reactions are those in which organic reactant react to form organic products.

Q: H2SO4 +

A: The reaction taking place is given as,

Q: What reagents are necessary to perform the following reaction? HO, Multiple Choice CH3CH2NH2, DCC

A: The carboxylic acid can be converted to Acid Chloride using the reagent Thionyl Chloride (SOCl2). In…

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.