2. Draw the carbocation intermediates (if any exist) and the products for each reaction. Include any intermediates and products arising from carbocation rearrangements. Be sure to include stereochemistry!!! 1. ВНз 2. H2О2, NaOн H2SO4 H20 Br2 HO, H2SO4 HO

Q: - please break down each step as much as possible, draw all possible products and consider…

A: DMSO is polar aprotic solvent , hence it favours SN2 reaction  In SN2 reaction nucleophile (RCOO-)…

Q: Which chlorination product is formed via the lowest energy transition state in the rate-determining…

A:

Q: please draw the starting materials for the following cycloadditions/ rearrangements. make sure to…

A: Since, you have multi subparts questions. So, I will solved first three subparts questions for you.…

Q: The following reaction can give two different mono-alkylation products depending on the conditions.…

A:

Q: Which compound would undergo carbocation rearrangement during an Syl reaction? Br Br A B Br C H Br D

A: Which compound would undergo carbocation rearrangement during an SN1 reaction? = B would undergo…

Q: 9. For the following carbocations: 1) determine if they rearrange, and 2) if they rearrange, draw…

A: Carbocation tends to undergo rearrangement reaction whenever there is a possibility of forming a…

Q: Cl Br А D E B

A: SN1 and E1 reactions is that SN1 reactions are substitution reactions whereas E1 reactions are…

Q: 4. (2 pts) Circle the most stable carbocation and cross out the least stable carbocation among the…

A:

Q: H CH,--CH, HS0, H2SO4 CH3-C-CH3 CH3-C=CH2 a. OH These 2 C's are identical. When either one loses a…

A:

Q: Draw the product formed from cyclohex-2-enone in each of three reactions. Reaction 1 Reaction 2…

A: Introduction: In the first reaction, cyanide ion act as a nucleophile attacks on the carbonyl…

Q: Could you also provide a brief explanation of what would happen to bromine when treated with…

A:

Q: Organic Chemistry Indicate which carbocation is the most stable carbocation and which carbocation is…

A: Carbocation :-  Ion with positive charge on carbon atom is called carbocation. The presence of…

Q: Br „CH3 CH3CH2OH H3C"

A: Organic reaction mechanisms

Q: te a full mechanism for each reaction shown below. (I) Clearl (iii) show stereochemistry where…

A: According to our guideline, I can answer only the first three sub-parts.

Q: Me Me Ме Me Ме H20 Br Br HO. + Но H Et Et RDS Et H Et Et transition state carbocation intermediate 우

A:

Q: Which cycloaddition reaction will proceed the FASTEST? Select one: `CHO OHC. Lons CH3 CHO

A: The given reaction is a Diels Alder reaction where substituted alkene (dienophile) reacts with the…

Q: Sometimes carbocation rearrangements can change the size of a ring.Draw a stepwise, detailed…

A: The formation of carbocation is shown below.

Q: In each box, provide either the missing reagents or the major organic product for each reaction…

A:

Q: hoose the compound below that gives a carbocation intermediate that undergoes rearrangement?

A: D will undergoes the rearrangement in intermediate of carbocation.

Q: Looking at the reaction below. Is A or B expected to be the major product and why? HO H H3C H3C. OH…

A: Base catalyzed ring opening of epoxide(oxiranes) takes place from the sterically less crowded side…

Q: Which reaction schemes is best to give the product? 2. HO. NO 2 O The following reaction scheme: Br2…

A:

Q: 6. Determine whether each reaction occurs by an Sn2, Sn1, E1, and/or E2 reaction. Provide a detailed…

A: Hello. There are multiple subparts to this question. The first three subparts have been solved. To…

Q: (i) which reaction among the pair, is fastest? Explain your (ii) predict the products of faster…

A:

Q: For the given reaction: ? HO ? + NaOH + NaCI + H2O Major substitution product Major elimination…

A:

Q: Br2 КОН 1. Na HNO3 Fe 2. EtBr H2SO4 HCI heat FeBr3

A:

Q: -PProvide reagents capable of accomplishing the transformations below. Some may require more th…

A: Organic reaction mechanisms:   As per our guideline we have to answer first three questions only.

Q: . Explain why do you choose that product and mechanism or in case something else happens explain…

A:

Q: Why do carbocation rearrangements occur? Choose all that apply. Ring strain can be reduced. They…

A: Carbocation rearrangements are the organic reactions in which the movement of an unstable…

Q: K (Most stable intermediate) CC, dil. H,SO, M N (Product) (Minor E1 product)

A: In this reaction first π bond breaks and H+ attack on anion and carbocation is formed which is 2°…

Q: What is a major product of the reaction sequence shown in the box? Br2 ? -Br Pd(OAc)2, K2CO3 Bu4NBr,…

A:

Q: 6. Determine whether each reaction occurs by an SN2, SN1, E1, and/or E2 reaction. Provide a detailed…

A: → In above base is weak so it show SN2 reaction.

Q: H F LL H LL F F

A:

Q: 4) Draw the major product of the following reactions (hint: watch out carbocation rearrangement): Br…

A: Given reactions are example of F.C. alkylation reaction.

Q: R OR1 -R2 R R-CEN

A:

Q: H. 1. CH3CH2CCLİ 2. Neutralizing work- dn

A:

Q: Identify the stronger nucleophile in each pair. a.NH3, −NH2 b.CH3NH2, CH3OH c.CH3CO2−, CH3CH2O−

A: -NH2 is a conjugate base of NH3. The amine-based compound is a stronger base than the alcohol-based…

Q: Draw all stereoisomers that can be produced in this reaction. CH,N2 (excess) ? hv

A: Given,

Q: Identify the stronger nucleophile in each pair. a. NH3,−NH2 b. CH3NH2, CH3OH c. CH3CO2−, CH3CH2O−

A: Nucleophile  : Molecule which easily donates electron pair are called nuclephile.

Q: The product in the following reaction is formed as a result of a 1,2-methyl shift from the initially…

A: The reaction takes place by formation of carbonation followed by migration of methyl group to come…

Q: Draw the elimination product for the following reactions. Identify which will be the main product…

A: According to Zaitsev rule, in elimination reaction most substituted product will be more stable and…

Q: Fill in the product, starting material, or reagent for each reaction. “No reaction" is a…

A: This is an example of conversion of alcohol to Chloro

Q: Which carbocation will rearrange? +) +) II A. Tonly B. Il only C. both I and II D. neither I or II

A: Answer :- I have explained each solution below hope this will help you !!!!!   Note - There will be…

Q: Drag the labels to identify the appropriate reagents for each reaction below. Each label is…

A: Double bond between two carbon atoms contain a 'pi' bond. The bonded carbons have sp2 hybridization…

Q: Rewrite each of the following stereospecific transforms as a synthetic step in the forward…

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

Q: 4. Circle the electrophilic and nucleophilic atoms in each substitution reaction below. Provide the…

A: We have to identify the electrophilic atom and the nucleophilic atom, also the stereochemistry of…

Q: Draw the TWO most abundant products for each reaction. Of the two products, circle the one product…

A: Given: Some of the Reactions are given To find: Products formed and circle the major product formed…

Q: This reaction can be completed with which reagents? (CH)CHCH;CH;c=CH (CH;),CHCH,CH;CCH: O H20,…

A: Hydration of alkyne

Q: What

A: We will write the product

Q: 3. What is the major product of this reaction sequence? CH-C%3С-НNaNH2, CH3B. H20, H2SO4 final II…

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.