н нн н ОН H3PO4 – H2O фа фан Н C н нн н + гар - Н a Major Н + офф (R) Н В trisubstituted A + tetrasubstituted Н Н н trisubstituted

Q: Draw the constitutional isomer formed in attached reaction.

A:

Q: Arrange the following compounds in order of increasing boiling point, briefly  explaining your…

A: When the crystals of any compound are impure due to any reason. They can be recrystallized by the…

Q: aromatic, anti-aromatic or neither.

A: To be aromatic, a molecule must meet the following four conditions: It must be a ring. It must be…

Q: Identify the anion as aromatic, antiaromatic, or nonaromatic. :o: aromatic antiaromatic nonaromatic

A: Answer : the given anion is Antiaromatic so, option b. Antiaromatic is correct

Q: Which one of these molecules are aromatic?

A: Aromatic compounds are those compounds that contain conjugated planar system with delocalization of…

Q: Provide the correct IUPAC name for the skeletal (line-bond) structure shown here.

A:

Q: Consider constitutional isomers only, ignore stereoisomers. a) b) The number of monochloro…

A: Givensome alkanesdetermine the number of monochloro substitution products.

Q: Draw the structure corresponding to following  IUPAC name. cyclobutylcycloheptane

A: The structure of the given IUPAC name can be drawn as

Q: C. H -H 'H 'С HI H Anisaldehyde Used in fragrence industry

A:

Q: Draw and name a constitutional isomer that is named a “....propyl...heptane”.

A: There are 3 position on which we can mame the compound as propyl heptane.

Q: CI Br

A: IUPAC (International Union of Pure & Applied Chemistry) naming rules are a standardized system…

Q: is there no steric strain between the ethyl and the hydrogen and the, propyl and the hydrogen?

A: IntroductionSteric strain refers to the repulsive interactions between bulky groups or atoms due to…

Q: the most reactive compound towards electrophylic addition reaction is: A) propyle chloride B)…

A: The objective of the question is to identify the most reactive compound towards electrophilic…

Q: When adding two equivalents of HBr to an alkyne, the second bromine will always add to the same…

A: When two equivalents of HBr is added to an alkyne then the addition follows markonvikov's rule. Two…

Q: Determine whether the following compounds are aromatic, anti-aromatic or neither. BH

A: Huckel’s Rule is used in order to estimate the aromatic qualities of any planar ring-shaped molecule…

Q: What happens to the number of H when introducing double bonds?

A: Since the double bonds are introduced in the compound means some bonds of the carbon is being broken…

Q: You will take advantage of the reactivities of these with either added acid or base. If they were to…

A: The question is asking why a product becomes soluble in the aqueous layer when it reacts with an…

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.