In the provided boxes, provide synthetic sequences (including reagents used and the compound produced in each intermediate step) for the following transformations.

In the space provided below, complete each transformation by indicating all necessary reagents, and/or the major organic product(s).

Draw the major organic product for the reaction shown. The starting material is a 5 carbon ring with a hydroxy substituent. This reacts with SOCl2 and pyridine to form the product.

Curved arrows are used to illustrate the flow of electrons. Using the provided starting structure, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. Then draw the organic product of this reaction. Include all lone pairs in the structures. Ignore inorganic byproducts, counterions, and solvents. H Na → Select to Add Arrows CH3CO2Na CH3CO2H 0:0 Select to Draw Product :O: :0: :0:

What is a major product of the sequence of reactions shown in the box? A) Br 이 ? Pd-cat, Base heat B) D)

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8) Show how the following conversions might be accomplished, including all reagents and intermediates. Br Y. OH

Chemistry please answer both in detail as im confused. thank you! Write the necessary steps to perform the following transformation. (Hint: This is a two-step procedure, H₂C For the reaction in problem 5, draw a stepwise mechanism for the first reaction

Provide TWO Grignard reactions, A and B, that can be to make the provided target structure. Give the organic reactant and the Grignard reagent that would be used, yo not need to specify the aqueous acid workup step, but you must specify which of the c-c bonds is being made in the provided traget structure. Ignore stereochemistry in this question.

Draw the products of the two step reaction sequence shown below. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts.