1. (3 pts) Atropine is easily racemized. Please provide a rationale AND a chemical mechanism for...
please help with part I and ii (b) According to the CDC, atropine and pralidoxime are antidotes for sarin toxicity (1)Briefly explain why atropine can be used as an antidote. (ii) Draw a chemical mechanism to demonstrate how pralidoxime chloride acts as an antidote. Me pralidoxime
Using the curved-arrow formalism, provide a mechanism that accounts for the following transformation. (5 pts) 1. OH НА OH 2. Using the curved-arrow formalism, provide a mechanism that accounts for the following transformation. (10 pts) H3O но C) OH
Question 8 1 pts The preoperative order is for atropine sulfate 0.15 mg. The supply of atropine sulfate is 0.4 mg/mL. How many mlL will you prepare? Please round to the nearest hundredth
10 pts. 5. Below is a reaction with a mechanism similar to the Hofmann rearrangement. Provide the mechanism and explain the purpose of the thionyl chloride. (8 pts.) NH2 OH 1. SOCI + CO2 2. Ho
Hello! Please illustrate detailed arrow-pushing mechanism for every step. Many thanks in advance! 2) Please provide the information asked for below. (Part A is 2 Pts. Part B is 10 Pts, Part C is 6 Pts, 18 points total). Су N=C=N a) -OH IZ 2 LN Provide the Product Common side product b) Provide a detailed mechanism for this amide formation. C) Account for how the side product is formed.
1. [05 pts.] Draw the chemical equation for preparation of Aspirin. (No mechanism) 2. [15 pts.) Show the detailed mechanism movement of electrons. for reaction. Show all arrow to indicate 3. [09 pts.] Briefly explain the roles of Salicylic acid, Acetic anhydride and phosphoric acid in the reaction. 4. [05 pts.] What type of reaction is preparation of Aspirin? 5. [06 pts.] Briefly describe esterification and give an example using Acyl chloride as one of the reactants.
please provide a full mechanism for the following reaction: 3) Provide a full mechanism to account for the product of the reaction shown below: o r _Naoip, Br * B Br Product Mechanism
(iii) Please predict the products and draw the mechanism for: 7.5 pts. H/CH OH 3
1. Provide a mechamism for the base promoted hydrolysis delta-valerolactone 2. synthesis (6 pts) BONUS 1: Mechanism: Provide a reasonable, detailed, stepwise mechanism for the base-promo hydrolysis of 7-valerolactone. 0 OH n + font + - сіз 602CH3 COM (3 pts) BONUS 2: Synthesis: 1. Na Cro 3. CH,OH, . A 4,4-dimethylpentan-1-01
(10 pts) 1 Mechanism - Carbonyl to imine Provide a reasonable detailed stepwise mechanism for the reaction of -toluidine with 3-pentanone initially be concerned about making the ketone a better electrophile.) Labelmportant intermediates) AS Oropriate show important resonance structures) (6 pts) 2. Nomenclature: Supply the IUPAC name for the following compound