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- Draw and label the chemical structure of the following reaction (include the curly arrow reaction mechanism): Tropine (CH (N)) + Ethyl Bromide (C_H_Br) 8 15 Intermediate → 2 → 5 Dolasetron (C1, H20203) (CHNO) 19 Tropine (C8H15N) + Ethyl Bromide (C2H5Br) Intermediate →Dolasetron (C19H20N2O3)What is the mechanism of this reaction?This reaction proceeds through a series of two elimination reactions. Which elimination do you believe is rate determining in this process and why?
- please DRAW out the full mechanism for this reaction. I will upvote responsesAnalyze the reactant(s) and reaction conditions, then predict the structure of the major organic product and indicate the predominant mechanism (SN1, Sx2, E1, or E2) of each reaction. Na OCH; CH;OH, 0° C CH;CH2CH2CH,Br Na SCH,CH3 DMF, 0° CIodination of acetone reaction is shown by the following equation. CH3COCH3 + I2 ⟶ CH3COCH2I + HI Therefore, − d [ C H 3 C O C H 3 ] d t is a correct expression that can define the rate of the above reaction. Is this true or false?
- What is the rate determining step for the reaction below? 0046 - 00905 + Hoy H IB کار تلوی 0 '애 + ation A B C D دو Acylium lon 0 COH + Multiple Choice: Only one answer is correct, and only one answer can be selected.How many steps in the mechanism of this reaction?H202 Ho write the mechanism of each reaction)
- Which step in the mechanism for free-radical bromination of propane is rate-determining? O Br-Br 2 Br O (CH3)2C-H+ Br→ (CH3)2C + HBr O (CH3)2C + Br-Br (CH3)2CBr + Br. O (CH3)2C + Br. → (CH3)2CBrprovide the complete reaction mechanism for each of the steps in the provided imageAnalyze the reactant(s) and reaction conditions, then predict the structure of the major organic product and indicate the predominant mechanism (S1, S2, E1, or E2) of each reaction. CHI CH₂SH 43°C