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- CH,CH,CI (5) ? AICI,OH O || CH,CHC-CH, Identify the appropriate bond(s) by selecting each atom individually on the canvas and assigning them a map number of 1 until all atoms of the bond are mapped. DQ ⓇH: 2N CONT NN 1. (1) A" ΔΕ OH O H₂C-C-C-CH₂ O O 0 Od H C N O S CI Br I P FC2H6 (1) O2 (g) -> CO2 (g) H:O (1) O2 (g) CO2 (g) H:O (1) CH4 (1) -> CHs (1) O2 (g) -> CO2 (g) H2O (1) NO:(g) O2 (g) N2O5 (g) heat
- :O: || H 4 'N• Ⓒ:O z: |||| :O I H อะเว: :CI:0 Q I I I I2 eq 1) NaOET. Постандот 3) НЗОЂMgBr Mg C,H,OC,H, MgBr o-CH O *MgBr C,H,OC,H, + CH,OH H,O, H,SO, O "MgBr OH Data Glassware oven-dried, assembled, placed under nitrogen (balloon). Materials: 10 mL anhydrous diethyl ether, 1.0 g Mg turnings. 4.5 mL bromobenzene. 10 mL more anhydrous diethyl ether. 2.5 ml methyl benzoate. Approximate initiation time: 15 min. Stir 10 min after addition of methyl benzoate. Transfer reaction mixture to 100 mL Erlenmeyer flask. Rinse reaction flask (2 x 20 mL diethyl ether). Acid quench solution: 25 mL 10 % aqueous sulfuric acid/15 g ice. Saturated NaCI solution: used 20 mL Hexanes: 20 mL Isolated: 1.82 g white solid What is the % yield of the reaction? What is the limiting reagent? Show complete calculations for the theoretical and % yield calculations
- Determine the hybridization of the central atom for each molecule. :ci: -AI- :CI: sp sp² sp³ O sp³d O sp³ d² -CI: sp sp² O sp³ sp³ d O sp³ d²Draw the following Lewis structures using condensed formulas. (a) нннн | | | | Н—С—С—С—С—н (b) нннн (c) | | | | Н-С—С—С—С—н H-C-H H H H H H H нн H H-C-C=ċ-ċ-H H. (d) H. (е) H (f) нн H. H-C-C Н-с—о—С-с-н H- C-C H-C. нн H. H-C. C- H H H. H нн H I- HIC-ISee image below
