Select the predominate product and determine the mechanism for the following reactions. OH OH SOCI₂ Pyridine Product 3 HCI Product 4 CI B CI D CI CI
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- Provide synthetic routes for the preparation of the starting materials of azo dye Alizarine Yellow R starting from benzene O₂N -NEN OH CO₂HProvide the mechanism for the following reaction (1) PhMgBr (2 equiv) (2) H3O+ workup OHESTIONS Predict the product formed in each of the following reactions and give each reactant and product a suitable name: 1) ether MgBr + CO₂ 2) H+ (a) (b) MO + D₂O MgBr 1) ether 2) H+ 1) ether 2) H+ (c) + CH2O MgBr (d) PhMgBr + =0 1) ether 2) H+ Labor
- Provide the major product for the following reaction? (1) Mg, ether (2) CO2 (3) H3O+* Predict the products and stereochemistry for the following reduction reaction NaBH4 (a) EtOH H2 Lindlar catalyst (b) 3-Hexyne (c) 3-Hexyne (d) CEC H2 Ni₂B (P-2) Na NH3Identify the major prouct of the folowing sololvsi reaction of 3bromo-1-methyiycopentene with methanol, Br CH,OH to
- Oct-1-yne (HC≡CCH2CH2CH2CH2CH2CH3) reacts rapidty with NaH, forming a gas that bubbles out of the reaction mixture, as one product. Oct-1-yne also reacts rapidty with CH3MgBr, and a different gas is produced. Write balanced equations for both reactions and identify the gases formed.Which of the following reactions will synthesize phenol from benzene? 1) HNO3 + H2SO4; 2) Fe, HCl; 3) NaNO2, HCl, 0-10 oC; 4) warm H2SO4 and H2O 1) HNO3 + H2SO4; 2) Fe, HCl; 3) NaNO2, HCl, 0-10 oC; 4) CuCN; 5) dilute acid and heat 1) Acetyl chloride & AlCl3; 2) bleach 1) Ph-N2+ + KI; 2) BrMgCH=CH2 in ether, followed by H3O+; 3) warm, conc'd KMnO4 1) Cl-CH(CH3)-CH2CH2CH3 + FeBr3; 2) hot, conc'd KMnO4Provide the structure of the major product(s) for the following reaction. || Ch₂ hv Na, CH,OH NH₂ 11 a Predict the product for the following reaction. II III C III IV IV