Devise a synthetic strategy to create the following compound, starting with ethyne and using any organic/inorganic reagents necessary. 3) НО. HO

Q: 1. A block of solid copper at room temperature is heated to 1200 degree celcius where it melts…

A: Explanations:A. physical change to the copper - is the correct answer because it melts only, melting…

Q: 4c. disubstituted benzene HO- HO. CI H2N

A: Disubstituted benzene :

Q: What is Aromaticity

A: Aromaticity is defined as a property of the conjugated cycloalkenes which enhances the stability of…

Q: 1) Write five

A: Carbon containing compounds are called organic compounds  Due to catenation property carbon can form…

Q: What are the properties of organic compounds?

A: Organic compounds The compound that contains Carbon and hydrogen are called organic compounds. Other…

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

A:

Q: Which class of hydrocarbon is saturated?

A: Hydrocarbons are compounds that contain only 'C' and 'H'. Several of them are used as fuels. The…

Q: What is the empirical formula for ethane, butane, and Ethyl ethanoate

A: We have to give the empirical formula for ethane, butane, and Ethyl ethanoate. Introduction: We know…

Q: of the following hydrocarbons are used as significant fraction of common gasoline. etylene opane…

A: The question is based on the concept of environmental chemistry. We  have to describe the…

Q: Table 1. Physical Properties SAMPLE DESCRIPTION(color, odor, clarity, physical state) n-Hexane…

A: General introduction: Physical property: Any measurable property is known as physical property. It…

Q: CH2-CH2-CH3 Type of functional group r. CH2-CH2-CH3 Common Name K* S. Type of functional group H3C…

A:

Q: and propane What is the relationship, if any, between these organic compounds? They are isomers.…

A: Isomers are compounds having same molecular formula but different structural formula. The chemical…

Q: 3. Differentiate the physical and chemical properties of the various organic compounds.

A: Among numerous organic compounds, the most important class of organic compounds include, Alcohols…

Q: What is your understanding of the term organic now ? Describe the connection you see between the…

A: A question based on nomenclature, which is to be accomplished.

Q: What is the practical importance of distillation in relation to pharmaceutical and medicinal organic…

A: In the modern organic chemistry laboratory, distillation is a powerful tool, both for the…

Q: Is C20H12 organic or not organic

A:

Q: 1. The torch used to start the modern Olympic Games uses a mixture of propane and butane. When…

A: A. Hydrogen and carbon. B. Hydrocarbons.

Q: Write the structural formula for butane and molecular formula?

A: Butane has 4 carbons and since it is a saturated hydrocarbon, thus, its molecular formula is…

Q: How many structural isomers can you draw for pentane?

A:

Q: what are all of the organic chemistry functional groups represented?

A: A functional group is an atom or group of atoms that determines the reactivity and the chemical…

Q: Write about the history of (Cyclohexene)? with book references

A: The aim of this question is to explain the history of cyclohexene, a cyclic hydrocarbon with the…

Q: Explain the process of polymerization and its significance in the formation of synthetic polymers.

A: Polymerization is a fundamental chemical reaction that involves the bonding of small molecules…

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.