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- If you were using the following reaction to produce acetone (CH3COCH3) CH3COCH2COOH → CH3COCH3 + CO2 what would be the overall atom efficiency of this reactionOCH3 + CH3NH2 a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown. • • • You do not have to consider stereochemistry. Do not include counter-ions, e.g., Na+, I, in your answer. In cases where there is more than one answer, just draw one. √n [ ? ChemDoodle b. Draw the structures of the organic products of the acyl transfer reaction. • You do not have to consider stereochemistry. • Draw the neutral form of the products: no charges.For the following unimolecular elimination reaction, draw the intermediate and the product(s) that would form. Include the correct stereochemistry in the product(s). + HCO; 0=$=
- When 2-chloro-2-methylpropane, (CH3)3CCl, reacts with aqueous sodium hydroxide, the process is not a “concerted process”; instead a reactive intermediate, (CH3)3C+, is formed as a result of the first step of the reaction mechanism. Explain why this happens.Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. (please show which structure I need to put as the answer).Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. You do not have to consider stereochemistry. Include all valence lone pairs in your answer.
- Help with this one please!7. For the following reactions: Draw ALL the products as required using any diagram type If more than one organic product forms, label the products as major, minor, or 50/50 Identify the general type of reaction (a) Reaction Type: H2 C. CH3 + Br2 (b) Reaction Type: AICI, Cl, (0)d) During the reaction between 3, 3-dimethylbutene (W) and HBr, intermediate species and Y are formed. CH3 CH;-C-CH=CH2 ČH3 HBr Y step 1 step 2 step 3 i) Write a mechanism for the formation of intermediate X? ii) Write the structure of intermediate Y? iii) Explain in your own words what happens in step 2 of the reaction? iv) Write a mechanism for the formation of Z from Y?
- Draw the structure of the organic product of the reaction between cyclohexene and OsO4, H₂O2. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. Separate multiple products using the + sign from the drop-down menu. • In cases where there is more than one answer, just draw one. ● MATIL ? Ⓡ ChemDoodle Sn [FDraw the structure of the major organic product(s) of the reaction. NaOH H20 CH3 • You do not have to consider stereochemistry. • All carboxyl and amino groups should be drawn in the neutral form. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in t Separate multiple products using the + sign from the drop-down menu. opy aste Cherr DbodleDraw the structure of the major organic product(s) of the reaction. malo H3C O ● • You do not have to consider stereochemistry. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu. *** 1. 2 H3C- 2. H30+ ChemDoodle -MgBr Sn [F