by elimination of an HCl molecule from a chloro-2-propane molecule is obtained: a) C2H4 b) C3H6 c) C3H4 d) C3H8

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A: when metabromo anisole is treated with ammonia reaction proceed through benzyne mechanism.

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A: Nitro benzene gives aniline in presence of SnCl2 with HCl

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Q: 76. Dienone phenol rearrangement reaction belongs to which type of reaction? A. Neutral B.…

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Q: When bromine adds to the double bond in a cyclohexene, the resulting  dibromide is trans. This…

A: When bromine adds to the double bond in cyclohexene, the resulting dibromide is trans. The reaction…

Q: O

A:

Q: Draw the organic product(s) of the following reaction. Aqueous H2SO4 H2N-N- + ethanol

A: Solution ;      Fischer indole synthesis: This reaction is one of the types of pericyclic…

Q: 19) Zaitsev's rule states that in substitution reactions, the most highly substituted alkene product…

A: False .

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Q: Draw the major organic product of the reaction shown below. CH3 HCI

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A: a) Please find the below pic for the reaction to for the above product.

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A:

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A:

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Q: 1. Write the correct IUPAC names for the following organic compounds: a) Br CH3 H3C (Assign E or Z…

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A: The reaction given is,

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Q: Bromoetherification, the addition of the elements of Br and OR to a double bond, is a common method…

A: To draw a stepwise mechanism for the below intermolecular bromoetherification reaction.

Q: 28. In the following reaction scheme which products are labeled correctly. Select all that apply.

A:

Q: Draw the structure(s) of the major organic product(s) of the following reaction. aqueous H2SO4 KCN

A: The reaction between a carbonyl compound and HCN is nucleophilic addition reactions. CN- acts as a…

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A:

Q: Select all of the compounds in the enol form of keto-enol tautomerism. он H.C. но HC HC, HC. CH,…

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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.