For each reaction, draw the complete mechanism and the major organic product(s), paying attention to stereochemistry. (a) (b) OH LOH (еxcess) ? ? CH,Cl2 CH2CI2
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- Predict the product(s) and provide the complete mechanism for each reaction below.For each section, circle the mechanism from the two options given (SN1 or SN2) and draw the main organic product resulting from that mechanism. Indicate the stereochemistry and if two configurational isomers form, draw both.Explain the following reaction with a mechanism.
- Draw the arrow-pushing mechanism and propose the products. When appropriate, make sure to indicate the appropriate stereo-/regio-chemistry of the product(s). Note that the mechanism(s) by which the product(s) form in reactions A and B are shown in pink. For Reactions C, D, and E you need to deduce the mechanism by carefully analyzing yout reagents and conditions.Cardura, a drug used to treat hypertension, is synthesized as shown here. a. Identify the intermediate (A) and show the mechanism for its formation.b. Show the mechanism for conversion of A to B. Which is formed more rapidly, A or B?Cardura, a drug used to treat hypertension, is synthesized as shown here. a. Identify the intermediate (A) and show the mechanism for its formation. b. Show the mechanism for conversion of A to B. Which is formed more rapidly, A or B?
- Draw the intermediates A-C for reactions a and b. Please show the appropriate stereochemistry where necessary.Provide a complete mechanism for the reaction, including all lone pairs, formal charges, andcurved arrows.Draw the product of this reaction and states its IUPAC name, and states what type of mechanism is occuring (eg. SN1, SN2, E1, E2, etc)?
- Provide the mechanism of the redica reaction below (b)3) Explain how and why the reaction below results in the observed regiochemistryand/or stereochemistry.Provide a detailed step-wise mechanism for the following reaction. Be sure to show all intermediates, formal charges, and show the movement of electrons with curved arrows.