(a-b) (c-d) (e-f) Predict the major organic products. H₂SO4 heat Br₂, FeBr3 SOCI₂ OH OH 1. NaH 2. CH3CH₂Br NH,NH2, KOH DMSO, (COCI) 2 Et3N

Q: Question 3 of 17 Provide the correct systematic name for the compound shown here. A OH trans- cis-…

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Q: (d) -CH,CH, (e) H CH,CH,CH=C-C-H ОН О CH,CHCH,C-OH

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Q: Q2 | Prepare the following Compounds ? 1-Asprin 2-Acetanilide 3-Phenol

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Q: Predict the major products.  Note: Write the name of the reactant and the product.

A: (g) When 2-butyne is treated with water in presence of Sulfuric acid and mercuric Sulfate, then…

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A: Solution: We know when haloforms treated with base (like NaOH) result in formation of carbene.…

Q: c) The reaction rate observed was 5 x 10-2 M.s¹ when the concentrations of A and B were 0.2 M and…

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Q: What is the major organic product produced by the reaction shown? CH3 CH3 (1) Os04 (2) NaHSO,…

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Q: show the major products

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Q: N₂ 1) Acetone H₂O C 2) CH (CO) NOCH, O A B. C. D E10₂C -CO,1 -CO,Et B) CO₂ NH COME CH coet

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Q: Provide the two major organic products of the following reaction. 3 AgNO3, H₂O

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A: Various Oxidizing  Agent and other Reagent  are used to  do following conversions

Q: H,C CH3 H&C C=C H;SO4 CH,CH,CHCH CH,CH,CHCH, C=C + CH,CH,CH=CH, + H +. 1-butene st H,0 H. CH3 H. 3%…

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Q: None

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Q: (f) bij Br 0 NaOCH₂CH₂ CH₂CH₂OH KHSO 4 heat косн сн. CH.CH OH KOCH(CH₂) + (CH) CHOH

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Q: Draw 4-ethylphenol (p-ethylphenol). Include all hydrogen atoms. OH What is wrong with this? H₂C ||…

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Q: H* a) CH,COOH H,C H20 b) CHy-C-H CHy-CH-CH2MGB. H* NABH,

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Q: Answer from left to right.

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Q: (a) (d) Excess HI Heat Excess HBr Heat ? ?

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Q: NaNH2 CH;CH,Br 1) О, cEC-H 2) Н.О (А) (В) TH. (С) (D) OH

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Q: 1) CH3-C-0 O 2) PHÁCH 13--0-C-CH3 3) H₂O 4) -H₂0 5) H O O O a) Ph-CH=CH₂ + CH3-C-OH b) Ph-CH=CH-C-OH…

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Q: Al₂(SO₄)₃ + 3Li --> 3Li₂SO₄ + 2Al Show the reactant and product.

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Q: (a) Determine the final products of the following chemical reactions. (i) CC4 + Br2 cyclohexene (ii)…

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Q: Acid 3- Fluro benzoic NO2 NO. NO2 Nitroben zene 1,3- Dinitro benzene HO. Final (3- Fluoro Fluero…

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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.