N(CH3)2 N(CH3)2 NHCH, F;C F3C KOC(CH)3 F3C one step CI но fluoxetine

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…

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

A:

Q: Draw a stepwise mechanism for the attached reaction, which involves two Friedel–Crafts reactions. B…

A: Various types of mechanisms are studied in organic chemistry. One of them is electrophilic…

Q: One step in the synthesis of the antihistamine fexofenadine involves acid-catalyzed hydration of the…

A: Acid catalyzed hydration of alkynes- Acid catalyzed hydration of alkynes produce ketone.…

Q: Draw a stepwise mechanism for the following reaction, which results in the synthesis of bisphenol F…

A: A stepwise mechanism for the given reaction can be shown below

Q: Draw a stepwise mechanism for the following substitution. Explain why 2-chloropyridine reacts faster…

A: Given reaction,

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

A: Given,

Q: Draw the organic products formed when attached allylic alcohol A is treated with following reagent.…

A: The addition of H2 in presence of a catalyst is known as catalytic hydrogenation reaction. This is a…

Q: Draw the organic products formed when attached allylic alcohol A is treated with following reagent.…

A: The given alcohol is a primary alcohol. PCC is a mild oxidizing agent. It is used to convert…

Q: Draw the products formed when A or B is treated with each reagent. In some cases, no reaction…

A: Hello. Since the question consists of multiple sub-parts, the first sub-part shall be only solved.…

Q: Draw the products formed when each ether is treated with two equivalents of HBr. a.…

A: The nucleophilic attack of the HBr on the electrophilic carbon favored the reaction. Ethers are…

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

A:

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

A:

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

A: This reaction is the electrophilic substitution reaction followed by basic medium

Q: Draw a stepwise mechanism for the formation of A from an alcohol and acid chloride. A was converted…

A: Since the alcohol group is having lone pair electrons and hence can attack on  electrophile And…

Q: Draw a stepwise mechanism for the formation of A from an alcohol and acid chloride. A was converted…

A: Since the alcohol group is having lone pair electrons and hence can attack on electrophile. Since,…

Q: Draw a stepwise mechanism for the following reaction.

A:

Q: Draw a stepwise mechanism for the conversion of lactone A to ester B using HCl in ethanol. B is…

A: In the first step of the mechanism the carbonyl group undergoes protonation followed by attack of…

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: Answer the following question about curcumin, a yellow pigmentisolated from turmeric, a tropical…

A: The enol form is more stable due to the intramolecular hydrogen bonding with nearby oxygen

Q: Devise a synthesis of each acetal from 1-bromo-2-methylhexane, alcohols (and diols) containing one…

A: The structure of 1-bromo-2-methylhexane is given as shown below. It consists of six carbon atoms in…

Q: Label the alkene in each drug as E or Z. Enclomiphene is one component of the fertility drug Clomid.…

A: a. The alkene in given drug Enclomiphene labelled as E or Z is shown below,

Q: Devise a synthesis of each compound from cyclopentanone, benzene, and organic alcohols having ≤ 3…

A: a. b.

Q: Draw a stepwise mechanism for the conversion of lactone A to ester B using HCl in ethanol. B is…

A: In the first step of the mechanism the carbonyl group undergoes protonation followed by attack of…

Q: What alkyl halides are formed when each ether is treated with HBr?

A: Alkyl ethers are cleaved by the strong acids HBr in a nucleophilic substitution reaction.…

Q: Draw the organic products formed when allylic alcohol A is treated with each reagent.a.H2 + Pd-C…

A: (a). Catalytic hydrogenation of allylic alcohol reduces the double bond to single bond giving…

Q: Draw the products formed when phenol(C6H5OH) is treated with each reagent. Give an explanation. e.…

A: FeBr3 acts as a Lewis acid and it reacts with Br2 and produces Br+ Phenol reacts with Br+ and…

Q: Two naturally occurring compounds that contain stable cyclic hemiacetals and acetals are monensin…

A: In acetal group , two ether linkages are present on the same carbon. In hemiacetal, one ether…

Q: Provide all possible products formed in the given reaction Draw the products formed when each ether…

A: When ether react with one equivalent HBr then alcohol and alkyl bromide is formed but when 2…

Q: Draw a stepwise mechanism for the following reaction that forms ether D. D can be converted to the…

A: Since KOC(CH3)3 is a strong base. Hence it will take proton from the OH group and convert it into O-…

Q: An allylic alcohol contains an OH group on a carbon atom adjacent to a C—C double bond. Treatment of…

A: The given reaction occurs via the formation of carbonation and this carbonation undergoes…

Q: Draw a stepwise mechanism for the following reaction that forms ether D. D can be converted to the…

A:

Q: Draw a stepwise mechanism for the attached reaction that forms ether D. D can be converted to the…

A: It is given that alcohol and an alkyl halide substrate are reacting to form an ether D, and further,…

Q: Draw a stepwise mechanism for the following reaction, which results in the synthesis of bisphenol F…

A: The organic reactions help in the synthesis of various new organic compounds.

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

A: The reaction of the carbonyl group with one mole of alcohol in the presence of the acid catalyst…

Q: Draw a stepwise mechanism for the conversion of lactone A to ester Busing HCl in ethanol. B is…

A:

Q: Provide a detailed, stepwise mechanism for the reaction shown below. CH3OH CH3 heat

A: From given reaction substrate and reagent. Generally allylic substitution reaction followed by SN2…

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

A: Step in the synthesis of the anti-inflammatory drug  Celebrex is shown below,

Q: 2. How many different ß-hydroxyaldehydes and ß-hydroxyketones, including constitutional isomers and…

A:

Q: Draw a stepwise mechanism for the formation of A from an alcohol and acid chloride. A was converted…

A: A species with a larger size can easily accommodate negative charge. In other words, in a large size…

Q: Two naturally occurring compounds that contain stable cyclic hemiacetals and acetals are monensin…

A: Carbonyl compounds and imide generally undergo a process called tautomerization. Tautomerization is…

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

A: The answer is attached below-

Q: How can pentan-2-one be converted to each compound?

A: Formation of the compound a from pentan-2-one is; Formation of the compound b from pentan-2-one is;…

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

A: This reaction mechanism contains two parts. First the dissociation of acetal into ethane-1,2-diol…

Q: Draw a stepwise mechanism for the following reaction.

A: Here the reactant present is 1,3-cyclohexadiene. The reaction undergoes in the presence of DCl ((2H)…

Q: Draw a stepwise, detailed mechanism for the following intramolecular reaction that forms a cyclic…

A: The given reaction is  To find: The stepwise mechanism for the given intramolecular reaction

Q: 4-Methylpyridine reacts with benzaldehyde (C6H5CHO) in the presence of base to form A. (a) Draw a…

A: a) A stepwise mechanism of the given reaction is,

Q: Draw the products formed when phenol(C6H5OH) is treated with each reagent. Give an explanation. c.…

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.