CI CH3 НО b. a. НО b.

Q: Draw a stepwise mechanism for the conversion of dihalide A and cyclohexane-1,4-diol to polyether B…

A: Since AlCl3 is a Lewis acid and hence it will extract Cl from the compound A forming a carbocation…

Q: What is the major alkene formed when A is treated with POCl3 andpyridine? Explain why the major…

A:

Q: Synthesize each compound from acetylene. You may use any other organic or inorganic reagents. C.…

A:

Q: Be sure to answer all parts. dentify the lettered compounds in the following reaction scheme. This…

A:

Q: QUE STION 23 Dehydration reactions ALWAY S form the most stable alkene as the major product. What is…

A: Dehydration reaction is the elimination of water molecule from a compound. Alcohols undergo…

Q: Draw the major organic product formed in the reaction. HBr -CH=CH-CH=CH2 (1 equiv.)

A: The reaction of alkene with HBr proceed through the formation of carbocation. if carbocation is less…

Q: Draw the structure(s) of the major organic product(s) of the following reaction. HCI + excess…

A: In the reaction between carbonyl group and alcohol, carbonyl group act as electrophile and alcohol…

Q: Draw the major organic product for each reaction. Assume a one-to-one ratio of starting material to…

A:

Q: Dehydration reactions ALWAY S form the most stable alkene as the major product. What is the major…

A: More stable alkene: Has greater substitution Bulky groups are on opposite side of double bond

Q: Convert each compound to its enol or keto tautomer. HO- a. b. CH CH3

A: The given compounds has to be converted into keto or enol form.

Q: Draw a stepwise mechanism for the dienone–phenol rearrangement, a reaction that forms…

A: A stepwise mechanism for the dienone–phenol rearrangement can be shown as follows,

Q: 1. Provide the missing product, reagent, or starting material for each reaction. CH3CH2ONA HO

A: All detailed  explanation  in Handwritten solution.

Q: 19) Zaitsev's rule states that in substitution reactions, the most highly substituted alkene product…

A: False .

Q: Draw the organic products formed when each alkyne is treated with two equivalents of HBr.

A: The reaction of alkyne with HBr is markovnikov reaction In this reaction negative part of the…

Q: 8.36 What is the major stereoisomer formed when each alkyl halide is treated with KOC(CH3)3? Br a.…

A: In chemistry, dehydrohalogenation is the process in which an elimination reaction removes a hydrogen…

Q: Compare These TWO reaction a and G Which both produces alkene Expluin what are the major differenLes…

A:

Q: O What is the term to describe the alcohol formation on the least substituted carbon of an alkene?…

A:

Q: Draw a stepwise mechanism for the conversion of dihalide A and cyclohexane-1,4-diol to polyether B…

A:

Q: Draw the products formed when each alkene is treated with NBS + hv.

A:

Q: What Wittig reagent and carbonyl compound are needed to prepare each alkene? When two routes are…

A: a.

Q: g) Convert propan-2-ol into the compound below. You can use any organic or inorganic reage (4

A: Here the question given propan-2-ol , so first we have to oxidized and ketone to formed. ketone…

Q: b H3C CH3

A: The reaction of an alkene with an acid is termed as halohydrogenation, which includes the breaking…

Q: Draw the major product of the reaction between 1-butanol and Na2Cr2O7, H2SO4, H2O.

A: 1-butanol is an alcohol having four carbon atoms.  It has the following structure: It is a primary…

Q: Draw the structure of the major organic product of the following reaction. CHз KMNO, heat н*

A: The reaction sequence is completed and products are identified in step two.

Q: Drawing the Products When Acetylide Anions React with Alkyl Halides Draw the organic products formed…

A: This is the nucleophilic substitution reaction where carbanion of acetylene attacks the…

Q: Draw a stepwise mechanism for the following reaction.

A: CrO3+H2O+H2SO4- The mixture of CrO3, H2O and H2SO4 is called as Jones reagent. Jones reagent is…

Q: 39) Why is there a need for a higher temperature set-up in elimination reactions? a. Because…

A: Elimination reactions are those reactions in which single bond is converted into multiple bond.  For…

Q: Synthesize attached compound from toluene (C6H5CH3) and any other organic or inorganic reagents.

A:

Q: (a) Add curved arrows for each step to show how A is converted to the epoxy ketone C. (b) Classify…

A: (a)  In this particular mechanism first the peroxide ion undergoes 1,4-addition with the reactant A…

Q: Label the a and B carbons in each alkyl halide. Draw all possible elimination products formed when…

A: Biomolecular elimination (E2) reaction: E2 reaction involves a one-step mechanism in which…

Q: CH2-C- CH3 - CH3

A: Given,  We have to synthesis the compound from alkyne and the corresponding reagents.

Q: (a) Add curved arrows for each step to show how A is converted to the epoxy ketone C. (b) Classify…

A: In this particular mechanism first the peroxide ion undergoes 1,4-addition with the reactant A to…

Q: Draw the starting structure that would produce this product under these conditions. Select to Draw…

A:

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

A: Hydroboration oxidation is an oxidation reaction of alcohols which convert alkenes to alcohol by…

Q: Draw a stepwise mechanism for the conversion of dihalide A andcyclohexane-1,4-diol to polyether B in…

A: The stepwise mechanism is given below -

Q: F. F SO3H SO3H A B

A: The above reaction is an example of electrophilic aromatic substitution.

Q: 29. Draw the major organic product of the reaction shown below. CH;OH CH3 H,SO4 CH3

A:

Q: Draw ALL possible elimination products and choose the one most likely formed and explain the reason.…

A: Here we have to predict the major product and possible elimination products obtained by the…

Q: OH CH3 H* H;CH,C ´OH

A: The reaction taking place is given as,

Q: Bromoetherification, the addition of the elements of Br and OR to a double bond, is a common method…

A: To draw a stepwise mechanism for the below intermolecular bromoetherification reaction.

Q: Draw the structure of the major product of 3-hexyne + 1 equiv HBr

A: When Alkyne reacts with one equivalent HBr then bromine atom attached to the most substituted carbon…

Q: 4. Show how to make each compound from an alkene (pay attention to regiochemistry) LOH OH

A: We have to draw the structures of the starting alkenes. And also we have to give the reagents.

Q: 69. When a straight cha in a lcohol is reacted with 12504, H3C-CH2-CH2-CH=CH, and H3C-CH2-CH=CH-CH3…

A: CH3CH2CH2CH(OH)CH3 + H2SO4 -----> CH3CH2CH2CH=CH2 + CH3CH2CH=CHCH3 Therefore, the original…

Q: 73. O-hydroxybenzoic acid is a major product formed with phenol and which other reactant/s?…

A: Here, we have to find the reagents that will convert phenol to o-hydroxybenzoic acid as a major…

Q: Organic Reactions: 1. Draw all potential products in the space below, for the alkane halogenation…

A:

Q: Axial alcohols are oxidized faster than equatorial alcohols by PCC and other Cr6+ oxidants. Which OH…

A: Three-dimensional structure of the molecules show how the possible arrangements actually are: a) The…

Q: 9.47 (a) What is the major alkene formed when A is dehydrated with H2SO4? OH A

A: The mechanism for this reaction is E1 (carbocation is intermediate which will go under…

Q: 31. What is the IUPAC name for the following compound? A) 1-Butyl-3-methyleyclohexane B)…

A:

Q: What steps are needed to convert Y to the alkene Z ?

A: Steps are needed to convert Y to the alkene Z has to be given.

Q: Draw a stepwise mechanism for the conversion of dihalide A and cyclohexane-1,4-diol to polyether B…

A: First the Lewis acid, AlCl3 takes chlorine from dihalide compound A results to form AlCl4- and…