CF3 OH CF3 CHNH2 (S)-fluoxetine

Q: Devise a synthesis of compound A from the given starting materials. You may use any other inorganic…

A: 3-hydroxy-4-methoxybenzaldehyde reacts with 1,3-dibromopropane in the presence of strong base like…

Q: One step in the synthesis of the antihistamine fexofenadine (Section 23.5) involves acid-catalyzed…

A: Given Structure: Reaction of A in presence of acid-calatysed hydration of H+ Following products are…

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A: The ion containing -ve charge over C-atom as well as a +ve charge over the heteroatom (S, N and P)…

Q: Which carbonyl groups in the anticancer drug Taxol will undergo nucleophilic addition, and which…

A: The nucleophilic addition is a characteristic reaction of carbonyl compounds. It is sensitive…

Q: Draw a stepwise mechanism for the following reaction, a key step in the synthesis of the…

A: Proton abstraction from the acid HCl. Nucleophilic attack on to the carbonyl carbon by the lone…

Q: Devise a synthesis of each compound from benzene. You may also useany organic compounds having four…

A: b.

Q: Devise a synthesis of each compound from the given starting materials. You may also use organic…

A: NOTE: Since, we only answer upto three sub-parts, we'll answer the first 3. Please resubmit the…

Q: „NH2 CH3 - aniline target compound CH3

A: In the given reaction the aniline is converted into the target molecule by several steps.

Q: A key step in the synthesis of the antidepressant paroxetine (trade name Paxil) involves a…

A: Alkyl halides undergo SN2 reaction with strong nucleophile to form ethers. This reaction is called…

Q: Bupropion, sold under the trade name of Zyban, is an antidepressant that was approved to aid smoking…

A: In the first step, benzene undergoes Friedel-Craft acylation to form propiophenone. The…

Q: Devise a synthesis of each compound using 1-bromobutane (CH3CH2CH2CH2Br) as the only organic…

A: Consider the given compound as a and b as shown below,

Q: Devise a synthesis of 2-methylcyclopentanone from cyclohexene. You may also use any required…

A: The reaction is,

Q: Draw a stepwise mechanism for the following reaction of a Grignard reagent with a cyclic amide.

A: Given,

Q: Devise a synthesis of muscalure, the sex pheromone of the common housey, from acetylene and any…

A: Please find below the reaction mechanism

Q: One synthesis of the cholesterol-lowering drug atorvastatin involves the construction of the pyrrole…

A: The organic conversions take place in more than one step with the help of various reagents.

Q: Devise a synthesis of optically active (S)-fluoxetine (trade name Prozac) from the given starting…

A: Given,

Q: Slow addition of organolithium reagent A to B afforded C, an intermediate in the synthesis of the…

A: Stepwise mechanism for this process can be drawn as

Q: Muscalure, the sex pheromone of the common housey, can be prepared by a reaction sequence that uses…

A: The formation of Muscalure follows a number of steps involving nucleophilic attack at the…

Q: Devise a synthesis of each compound from aniline (C6H5NH2).

A: The substitution on aniline is achieved via Friedel-Crafts reaction. The amine group present in…

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A: The carbon compounds which contains –CO- group are termed as ketones. They are also named as the…

Q: Kindly draw the product that was fromed when phenylacetic acid was treated with the reagent, show…

A:

Q: Suggest a synthesis of the following compound by Claisen or Dieckmann condensations. Show all…

A: It is Claisen Condensation reaction. It is a base catalysed reaction. Reactant is ester.

Q: Attenol A and pinnatoxin A are natural products isolated from marine sources. (a) Locate the…

A: The diether derivates of the aldehydes and ketones are known as acetals or ketals. The imine is a…

Q: Treatment of ketone A with LDA followed by CH3CH2I did not form the desired alkylation product B.…

A: The product formed in the reaction is shown below.

Q: Draw a stepwise mechanism for the intramolecular Friedel–Crafts acylation of compound A to form B. B…

A: Concept introduction: The Friedel-Craft acylation is a type of electrophilic substitution reaction.…

Q: Draw a stepwise mechanism for the sulfonation of an alkyl benzene such as A to form a substituted…

A: Stepwise mechanism for the sulfonation of alkyl benzene to form a substituted benzene sulfonic acid…

Q: Devise a synthesis of the following compound. You may use HC=CH, ethylene oxide, and alkyl halides…

A: Acetylene (C2H2) contains two acidic hydrogens in presence of strong base like NaH it gives…

Q: Consider the two-step synthesis of 2-hydroxy-2,4-dimethylpentanoic acid using the reagents provided.…

A: The prussic acid is another name of hydrogen cyanide having formula HCN. This hydrogen cyanide is a…

Q: (R)-Carvone, the major component of the oil of spearmint, undergoes acid-catalyzed isomerization to…

A: Acid-catalyzed isomerization of R carvone leads to the product carvacrol which is more stable than…

Q: Devise a synthesis of each compound using 1-bromobutane (CH,CH,CH,CH,Br) as the only organic…

A: Use a staring material 1 bromobutane and reagents use give in question product formation

Q: Propranolol, an antihypertensive agent used in the treatment of high blood pressure, can be prepared…

A:

Q: 2b. Device a synthesis route for the following: Hg(OAc): NaBH, он p-TSCI pyridine a) b) KCN d)

A: Oxymercuration reaction: The alkene gives an electrophilic addition reaction to form alcohol. When…

Q: A key step in the synthesis of β-vetivone, a major constituent of vetiver, a perennial grass found…

A: LDA acts as a bulky base. It abstracts the ‘H’ from the less hindered site. Step wise mechanism for…

Q: Devise a synthesis of each compound using 1-bromobutane (CH3CH2CH2CH2Br) as the only organic…

A: Consider the given compound as A and B as shown below,

Q: Devise a stepwise mechanism for the following reaction.

A: Please find below the reaction mechanism

Q: Devise a synthesis of each compound from benzene, any organic alcohols having four or fewer carbons,…

A: a.

Q: Devise a synthesis of compound A from the given starting materials. Youmay use any other inorganic…

A:

Q: Devise a synthesis of each compound from benzene using a Suzukireaction. You may also use organic…

A: Given compounds,

Q: β-Vetivone is isolated from vetiver, a perennial grass that yields a variety of compounds used in…

A: a.

Q: 4. Devise a forward synthesis given the retrosynthetic analysis, only using the starting materials…

A: Introduction: Suzuki reaction: It is cross coupling reaction of a boronic acid with a halide or…

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A: The reactions involving organic compounds are called organic reactions. Electrophilic and…

Q: The pKa of p-cyclopropylbenzoic acid is 4.45 . Is cyclopropylbenzene likely to be more reactive or…

A:

Q: Devise a synthesis of each compound from aniline (C6H5NH2) as starting material.

A: Chemical synthesis is the sequential formation of the desired product with the fixed sequence of…

Q: Draw a stepwise mechanism for the intramolecular Friedel–Crafts acylation of compound A to form B. B…

A: The stepwise mechanism is shown below,

Q: (R)-Carvone, the major component of the oil of spearmint, undergoes acid-catalyzed isomerization to…

A: The protonation of (R)- carvone is show below.

Q: Devise a synthesis of anastrozole, a drug used to reduce the recurrence of breast cancer, from the…

A: Anastrozole is a Aromatase inhibitor used in the treatment of breast cancer.

Q: Draw a stepwise mechanism for the intramolecular Friedel–Crafts acylation of compound A to form B. B…

A: Friedel-Crafts Alkylation is used to alkylate aromatic compounds like benzene. This reactions makes…

Q: Devise a synthesis of each compound from benzene and organic alcohols containing four or fewer…

A:

Q: 22. Provide the following: 1) the major organic product of each reaction shown, and ii) the specific…

A:

Q: Devise a synthesis of each compound from aniline (C6H5NH2).

A: Given compounds,

Amines

Amines are organic compounds with a nitrogen atom having a lone pair of electrons on it. They are derived from ammonia (NH3) wherein hydrogen atoms are substituted by an aryl or alkyl group.