Which of the following reactions will not generate an alcohol group in the product? (1) CH; CH,MgBr Reaction A (2) dil. H*/H;O NaOH Br Reaction B H20/THF (1) Hg(OAc)2/ H20 Reaction C (2) NABH/ethanol NaOH Reaction D H20/THF Reaction B Reaction A Reaction C Reaction D
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- What is the structure of compound A? 010 Compound A tot 01 Oll O III O IV OV || s ||| Compound A IV COOHWhat is the predicted product of the reaction shown? I H Na2Cr₂O7/H2SO4/H₂O || OH OH ||| LOH of or H IV V OHDiaw structural formulas for the major organic producto 9) MCH SOCI₂ b) 2) d) SE охон a OH HCl OH HBr excess H₂ CrOA HIOA DOD4, HD₂ HIO pruch, THEO 2) ft₂N for each reaction.
- write the tollowing equatios and, De lermine which the ty pe A reactin ard mechun's m ifa CHe- I Hcl 3. ethanivl> ethanal KOH + Nacw- ee ethanol19. Which of the following compounds has the LOWEST solubility in water at 25 °C? a) CH;CH;CH;OH b) CH-CH:CH:CH.ОН c) CH3CH2CH2CH;CH2OH d) same solubility for all19. What is(are) the major organic product(s) of the following reaction? O III CH₂CH₂CH₂CCI b CII CO₂Na 00 11 11 A) CH-CH₂CH₂COCCH; oled nworla bruoqmos en a B) CH;CHẠCH CONa + CH, CC1 nefeeofol 0.8 ||| C) CH₂CH-CH-COCH, obby D) CH CH CH CCH, enclosi.A enotexlib O
- Provide structures of the reactant/products: a) но. 1. D -MgBr 2. H3O* H 1. LIAIH4 2. H30* b) OH c) H. H* H* acetal OH OH H* H* acetalWhat is the intermediate before the final product of the following reactions? ii NaOH H* heat O a. Na Ob. OH OH Od. Na* он e. Of.CH;-CH,-CH2-C-OH b. CH3-CH-C-0OH each of the following С. А с. JUPAC Nomenclature for Carboxylic Acids (Section 5-2) 5-13 Give the IUPAC name for each of the following carboxylic acids. 1- que CH3 0 o a. CH3-CH2 O c. CH3-CH2-CH-C-OH d. CH3-CH2-COOH miado obia (0-2 noito na sisibio n o gnot
- Reaction C Select Draw Rings More |||||| C 0 N H 0 || H H₂C C-C I heat H₂C CH–COOH +CH,CH(CH,)NH, H₂C- CH₂ H₂C J Q2Q Draw the amide formed when isopropylamine (CH₂CH(CH³)NH₂) (CH3CH(CH3)NH₂) is heated with each carboxylic acid. Include all hydrogen atoms. What did I do wrong? N HC- Erase CH₂The 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?7) Provide the structure of the major organic product in the following reaction. HOT 7a) 7b) 7c) CH3 H3CO. H3CO. H3CO. CI. H. CN X· X- NC H 7d) H3CO CI CO₂CH3 A A A