Determine the type of alcohol represented by each structure.

Q: CH3-CH2-CH,-CH2-CH2-Ĉ-H

A: Select the longest carbon chain as main chain  Numbering (it starts from carbonyl carbon)  Naming…

Q: raw structural formulas for this compound . Q.)Cyclohexene oxide

A: Cyclohexene oxide is a cyclic hydrocarbon whose functional group is epoxide. This is used as an…

Q: Classify the following Alcohol, Phenol, Thiol, Ether, Aldehyde as an or Ketone.

A:

Q: Comparing Hexane and Dimethyl ether, why does dimethyl ether have weaker intermolecular forces than…

A: The hexane has the stronger attractions between its molecules through London dispersion forces.…

Q: HO

A:

Q: Determine methanes boiling point and melting point.

A: Boiling point depend upon the intermolecular forces stronger the intermolecular forces more is the…

Q: c Draw the 'dot-and-cross' diagram for one molecule of propene.

A: Given,  Propene (CH2=CH-CH3)  Structure,

Q: Name attached ether, epoxide, thiol, and sulfide.

A:

Q: 1. Alcohols are viewed as alkyles derivatives of water Draw water and an alcohol next to it, compre…

A: Hello. Since more than one question has been posted, the first question shall only be solved in this…

Q: Question 39 The skeletal formula represents what type of alcohol? HO. A) primary B) secondary C)…

A: The question is based on the concept of Alcohols. we have to identify the type of alcohol given in…

Q: Draw an example of each of the following molecules a) Alcohols b) Aldehydes c) Carboxylic acids d)…

A:

Q: Which of the following statements is true of dimethyl ether and ethanol?     a)  The boiling points…

A: dimethyl ether and ethanolWe need to comparison the boiling point between dimethyl ether and ethanol…

Q: What type of molecules do organic chemists study?

A: Organic chemistry is a branch of chemistry.

Q: Ketone with at least three carbon atoms

A: The question is based on the concept of organic chemistry. we have to write the molecule with having…

Q: Following is the structure of cortisone, a corticosteroid that increases the blood glucose level and…

A: The structure of cortisone is given. We have to find the functional groups in the structure

Q: Define Methanol (CH3OH)

A: Given Define Methanol CH3OH

Q: Identify an incorrect statement concerning the physical properties of alcohols.

A: We can attribute this to the presence of intermolecular hydrogen bonding between hydroxyl groups of…

Q: OH Determine the type of alcohol the molecule shown here. A) primary B) secondary C) tertiary D)…

A: Note: As per our guidelines, we are supposed to answer only one question when multiple questions are…

Q: What intermolecular forces are present in the alcohols?

A: Intermolecular forces are the attractive force that withholds two molecules is called as…

Q: 1. Provide the IUPAC name. a. H3CO. F IUPAC name

A: The given compounds are derivatives of benzene. The IUPAC name of the benzene derivative is given…

Q: Alcohol with at least three carbon atoms

A: The alcohol is the functional group . In the alcohol the OH group is attached to the  carbon atom .…

Q: What is an alkyl group? How is a given alkyl group related to its parent all and?

A: A type of functional group that contains only hydrogen and carbon atoms in its structure is said to…

Q: name only functional group

A: First is ether functional group. Oxygen bonded with two carbon atom via single bond.

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.