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?a) Propose the products of the following reactions of Lactone P. T 1. LIAIH,, ether 2. Н.О 1. DIBAL S NaOH H;O* 2. H;O* Lactone (P) 2 CH,MgBr