Ethynylcyclopentane, first reacts with sodium amide. The product formed in the first step reacts with bromocyclohexane in the second step. What is the final major product of these reactions? 1) NaNH2 2) CH,Br II IV

Q: РСС, THF 1) NaH Na,Cr,O, 2)CH3CH2CH2BT OH H;0", THF, 25°C PB13 POC13, pyridine, 0°C

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Q: Propose a series of reactions that would convert the provided starting material into the given…

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Q: I 1. NaNH, 2. CH3CH₂ NH₂ II E III IV

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Q: Br + S: Na* 11 {= IV Br

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A: These are the examples of aromatic electrophilic substitution reactions

Q: QUESTION 6 Identify the reagents and the compounds from A to E? Br A Mg/Ether CH2OH B CH3NH2 CHO E…

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Q: Which reagent(s) will complete the following reaction? OH ✗OH H2SO4 H2SO4 AICI 3 AICI 3 11 III IV IV…

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Q: What is the product using these reagents? 1) Mg, Et2O; 2) D2O.

A: The Answer to the following question is-

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Q: 4) Which alkene reacts with CH₂OH in the presence of an acid catalyst to give CH₂ H₂C-C-0-CH₂? CH₂…

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Q: How many different products (excluding stereoisomers) are expected in this reaction? HCI ? 1 2 3 4 5

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Q: Name this compound according to the IUPAC system, including stereochemistry. Br CH 2,6-dibromo

A: Name the given organic compound include stereochemistry---

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A: An allylic carbon is a carbon atom bonded to a carbon atom that is bonded to another carbon atom.

Q: WHAT REACTANTS WOULD GIVE THE FOLLOWING PRODUCTS? C8O2+NH(CH3)3

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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.