pyridine reacts with 1-bromobutane to give?

Q: The analgesic naproxen can be prepared by a stepwise reaction sequence from ester A. Using enolate…

A: The most acidic proton in compound A will be the one which is attached to the carbon adjacent to the…

Q: What products are obtained from the reaction of cyclohexene oxide with a. methoxide ion? b.…

A: a) Please find below the reaction. The methoxide ion attacks the C on cyclohexene oxide and opens…

Q: What product is obtained from the reaction of excess benzene with isobutyl chloride + AlCl3 ?

A: The reaction of isobutyl chloride in AlCl3 with benzene is an electrophilic substitution reaction.…

Q: benzene to p-bromobenzoic synthesis

A: Answer is explained below.

Q: Sulfur ylides, like the phosphorus ylides of Chapter 21, are useful intermediates in organic…

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

Q: an oxidizing agent KMNO4/H2SO4 and resulting product is treated with NH3. (i) Ethanal is oxidized by

A: In other words, the oxidising agent is a material that has the ability to oxidise other compounds to…

Q: What is the major organic product obtained from the following reaction? B

A:

Q: Why does phenol or aniline react with benzene diazonium chloride during a coupling reaction, but…

A: It can be easily explain by  with help of mechanism. In case of phenol and aniline the benzene ring…

Q: (a) Give mechanism of preparation of ethoxy ethane from ethanol.(b) How is toluene obtained from…

A:

Q: Two isomers, A and B, of molecular formula C5H8 undergo catalytic hydrogenation with hydrogen gas…

A: So here, we have to calculate 1st the double bond equivalent.

Q: Show how the aniline can be prepared from benzene:

A:

Q: Two isomers, A and B, of molecular formula C5H8 undergo catalytic hydrogenation with hydrogen gas…

A:

Q: The analgesic acetaminophen is synthesized by treating 4-aminophenol with one equivalent of acetic…

A: Given 4-aminophenol + acetic anhydride ----> acetaminophen + additional product

Q: Consider the following reaction: 2- bromooctane reacted with Sodium tert-butoxide complete reaction…

A: 2-bromooctane + sodium tert-butoxide --> ->Sodium tert-butoxide has more basic character than…

Q: (a) Synthesis of ethanol from the corresponding oxo compounds with Grignard reagent  b) Formation of…

A:

Q: Devise a synthesis of this compunds from benzene with reagents 2-propyl-4-chlrobenzenesulfonic acid

A: The synthesis of 2-propyl-4-chlorobenzenesulfonic acid from benzene has to be given.

Q: Outline a synthesis of each Wittig reagent from Ph3P and an alkyl halide.

A: Given:

Q: Aromatic substitution can be done on naphthalene. Treatment of naphthalene with concentrated H2SO4…

A: The two compounds are 1-naphthalenesulfonic acid and 2-naphthalenesulfonic acid. The sulfonation of…

Q: What product is obtained from the reaction of excess benzene with dichloromethane + AlCl3 ?

A: Given reactions, Reaction of benzene with Dichloromethane + AlCl3   Product of the given reactions,

Q: Ethanal reacts with semicarbazide and resulting product is boiled with aq. KOH

A: Semicarbazide is an ammonia derivative of the formula, H2NNHCONH2.Aldehydes undergoes a condensation…

Q: What reaction do nitro compounds undergo when treated with reducing agent?

A:

Q: n synthesis of benzoic acid with Grignard reagent, benzene is often detected as an impurity. How is…

A: Grignard Reagent  Are very Powerful  base which Takes Place H+  From solution  and get converted…

Q: Carboxylic acids are lowest in reactivity towards nucleophilic substitution. Why? (Consider the…

A:

Q: What is the major product formed, when toluene undergoes Friedel-Craft's alkylation with vinyl…

A: Friedel-Crafts Alkylation reaction is the reaction of toulene with haloalkanes in presence of…

Q: Prepare m chloroacetophenone from benzene using the necessary reagent

A: Meta-chloroacetophenone from benzene has to be prepared using the necessary reagent .

Q: Express the reaction of α,β-Unsaturated Carbonyl Compounds with Organometallic Reagents ?

A: Grignard reagent reacts directly with the carbonyl C, that is, it shows 1,2 addition. Gilman reagent…

Q: ompounds: trinitrophenol Illustrate all the possible reaction for toluene. b. dichlorobenzoic acid…

A:

Q: Benzoic acid is treated with SOCI, and the product (X) formed is reacted with ammonia to give (Y).…

A:

Q: Chlorobenzene is extremely less reactive towards a nucleophilic substitution reaction. Give two…

A: There are some electron displacement effects like , resonance effect, inductive effect etc. decides…

Q: غير مجاب علیه بعد سؤال 7 الدرجة من 2.00 Acetylene reacts with water in the presence of sulfuric acid…

A: Hydrocarbons are defined as organic compounds which are solely made up of carbon and hydrogen atoms.…

Q: Synthetize 3-pentynal from 3-butynal using whatever organic/inorganic reagents are needed.

A: Organic reaction mechanisms:

Q: a) Wolff-Kishner reduction of compound W gave compound A. Treatment of A with m- chloroperbenzoic…

A: Oxidation and reduction are common class type of organic reactions. In oxidation reaction, oxygen is…

Q: (a) Explain the mechanism of a nucleophilic attack on the carbonyl group of an aldehyde or a…

A: The carbonyl group in an aldehyde or a ketone is highly polar in nature. Because the carbon atom of…

Q: Bromocyclopentane is more reactive than bromocyclohexane when heated with sodium iodide in acetone.…

A: Given: Bromocyclopentane is more reactive than bromocyclohexane when heated with sodium iodide in…

Q: The following product was obtained from the ozonolysis of an alkene followed by treatment with…

A: Ozonolysis of alkene is the reaction of alkene with ozone forms ozonide this on further hydrolysis…

Q: Explain the Limitations on Electrophilic Substitution Reactions with Substituted Benzenes ?

A: Electrophilic Substitution reactions are the most important and characteristic reactions of Benzene…

Q: Please draw reaction out of:  prop-1-yne reacts with H2 and palladium on carbon  butan-2-one…

A: H2 and Pd/C reduce alkyne completely into alkane  Sodium bromohydride (NaBH4), being a mild reducing…

Q: from the reaction of elimination of two moles of water from one molecule of ethanediol when treated…

A: An elimination reaction is a form of organic reaction that removes two substituents from a molecule…

Q: Two isomers, A and B, of molecular formula C5H8 undergo catalytic hydrogenation with hydrogen gas…

A: Given are two isomers of C5H8.

Q: ethers can often be prepared by Sn2 reaction of an alkoxide and alkylhalides, which is a better…

A: In the Williamson synthesis, either is formed, in the reaction between alkoxide and alkyl halide.…

Q: How would you convert the benzene into cinnamic acid?

A:

Q: What are the various functions of phenolics and Give seperately industrial uses of phenolics. Answer…

A:

Q: The analgesic naproxen can be prepared by a stepwise reaction sequence from ester A. Using enolate…

A: The most acidic proton in compound A will be the one which is attached to the carbon adjacent to the…

Q: Provide all resonance structures of the sigma complex when aniline reacts with an electrophile to…

A: Reaction is taking place between aniline and Br2 (Br electrophile)

Q: Nerol, a natural product from lemongrass, can be converted to α-cyclogeraniol upon treatment with…

A: Given reaction,

Q: product formed by treating butanal with 1. AgNO3 in HH3 2. Acidified K2CrO4 3. LiAlH4

A: Organic compounds are the compounds which are mainly composed C and H atoms. The branch of chemistry…

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.