H -OAC Drag To Par HO HO HO H H нон Draw the product of the reaction below. Ignore inorganic byproducts. HO HOH H OAC H OHI OH H Q excess CH3I Ag2O H H H IT H H H Drag To Pan
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- Saaly ikäi Give a systemic name for each compound ОН (f) OCHWhich of the following will be the dominant product of the dehydration reaction shown? H;PO, H2O. A но (A) (B) (C) (D) Compound B Compound C OCompoundD OCompound A nintc)10:08 24 of 51 Done Which is true of the reaction? NAOH The reaction proceeds by an E2 mechanism, and the reaction rate is first order in alkyl bromide concentration and independent of hydroxide concentration. a. Ob. The reaction proceeds by an E2 mechanism, and the reaction rate is first order in both alkyl bromide and hydroxide concentrations. The reaction proceeds by an E1 mechanism, and the reaction rate is first order in alkyl bromide concentration and independent of hydroxide concentration. The reaction proceeds by an E1 mechanism, and the reaction rate is first order in both hydroxide concentrations.
- 23. What product is formed when the following substance is treated with CrO3 under appropriate conditions? a) que H b) O OH c) O d)What is the basicity of H2SO4Chapter 8 66) Dip henhy dia mine , the two-step seguence What is the structure antihistamine following in Bena dry l, can be pre pared by the di phenhy dra mine of HUN [1] Br diphenhy dramine Ho. [2] no substi tion veaction
- 8) OH ел 'H HCI H2O W How many stereoisomers are possible for this cyclic hemiacetal? OHStep 2: A hemiacetal formation has a similar mechanism to the hydrate reaction, except 1 equivalent of alcohol is added instead of water. 1² R₂ R₁ LOR3 R₁ R₂ The hemiacetal reaction is also reversible and can also be catalyzed by either acid or base. Hemiacetals are not usually isolated, except in the formation of 5- and 6-membered rings, as often seen in carbohydrate chemistry. Identify the hemiacetal formed from the intramolecular cyclization of the molecule shown. OH H OH R3OH OH OH OH CH₂OH NaOH ?2. For the following amines A and B, show all of the Hoffman elimination products. If one product is favored, please indicate it as the major product. CH₂ A920A pirtw sont at quo antsvorg is a quang how off siism enw secolabixosbyd mulboe Biw thouƏTİ aqada notibadongsb bas 00
- The key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold Helminthosporium sativum, involves the following base treatment of a keto tosylate. What kind of reaction is occurring? How would you complete the synthesis?Thioglycolic acid, HSCH2CO2H, a substance used in depilatory agents (hair removers) has pKa = 3.42. What is the percent dissociation of thioglycolic acid in a buffer solution at pH = 3.0?When a carboxylic acid is dissolved in isotopically labeled water, the label rapidly becomes incorporated into both oxygen atoms of the carboxylic acid. Explain.