H H H CH3 Br Draw Substitution Product dissociation CH3CO2Na CH3CO2H Select to Draw Carbocation Intermediate 1,2-hydride shift H H

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Q: IX. Devise a synthesis for cyclohexene from the compound shown. You may use any other organic or…

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Q: Nitrosyl bromide decomposes according to the following equation: 2NOBr (g) ⇌ 2NO (g) + Br2 (g) A…

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Q: -ОН 1. Na2Cr2O7, H2O 2. NaOCH3, CH3OH

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Q: Consider the rate law, (Look at the picture) How does the rate change when the concentration of [H+]…

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Q: A mixture is 18.7% NaCl, 20.6% CaCl2, and 60.7% NaBr. What mass of the mixture contains 0.454 moles…

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Q: A monatomic ion with a charge of +2 has an electronic configuration of 1s²2s²2p63s²3p64s²3d¹04p6.…

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Q: Trial 1 2 3 [A] (M) 0.200 0.400 0.200 A+BAB What is the rate constant for the reaction above? [B]…

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Q: O CH3-C-0-H + CH3CH₂ CHCH₂OH I CH₂CH3 6 11 ECH3-C-O-CH2CHCHACH3+H2O CH₂ CH3

A: The reactants given are acetic acid and 2-ethylbutan-1-ol.

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A: Given The pH of a 0.100 M aqueous solution of an unknown monoprotic acid, HX, is 5.26 at 25 ºC Ka =…

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Q: Given 100.0 mL of a buffer that is 0.50 M in HOC1 and 0.60 M in NaOC1, what is the pH after 20.0 mL…

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A: Acids- donate H+ ions  Base - donate OH- ions

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Q: At 27 °C, K₂= 1.5 × 1018 for the reaction 3NO(g) N₂O(g) + NO₂(g) If 0.030 mol of NO were placed in a…

A: The given reaction is: 3 NO(g) ⇌ N2O(g) + NO2(g) Kp = 1.5×10^18 at 27°C.

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.