Please explain why C and D are the precursors ### Reaction Scheme OverviewThis diagram depicts the synthesis of an alcohol from its immediate precursors. The main components shown include the target alcohol and several possible precursor compounds labeled A through F.#### Target Alcohol:- **Chemical Structure:** A secondary alcohol with an OH group attached to a central carbon. This carbon is bonded to two phenyl rings (aromatic benzene rings), making it a biphenyl alcohol structure.- **Label:** Alcohol#### Possible Precursors:1. **Structure A:** - Contains a benzaldehyde moiety. - Features an aldehyde group attached to a phenyl ring.2. **Structure B:** - A Grignard reagent, specifically ethylmagnesium bromide (CH₃CH₂MgBr).3. **Structure C:** - Another Grignard reagent, phenylmagnesium bromide, with a phenyl group attached to magnesium bromide.4. **Structure D:** - Contains a benzaldehyde moiety with an aldehyde group on a different side compared to structure A but similar in format.5. **Structure E:** - Features acetaldehyde, an aldehyde with a methyl group attached to the carbonyl group.6. **Structure F:** - A Grignard reagent with benzylmagnesium bromide, having a benzyl group attached to magnesium bromide.### Conclusion:This diagram illustrates the choice of chemical precursors that could potentially undergo a reaction to form the target alcohol through Grignard synthesis. The conversion involves the reaction between a Grignard reagent and a suitable carbonyl-containing compound.

Answered: OH + alcohol immediate precursors MgBr…

OH + alcohol immediate precursors MgBr CH3CH,MgBr A B H. `MgBr H3C D E F

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

Similar questions

Give typed full explanation not a single word hand written otherwise leave it
For the following SN2 reaction, draw the major organic product and select the correct (R) or (5) designation around the stereocenter carbon in the organic substrate and organic product. Include wedge/dash bonds and H on a stereacenter. J H The correct (R) or (S) designations for the stereocenter carbons are: The organic substrate is (S) and the organic product is (R). The organic substrate is (R) and the organic product is (S). The organic substrate and organic product are both (S). The organic substrate and organic product are both (R).
4. Draw all products for each of the following reactions or reaction sequences. For chiral molecules that are racemic, you needn't draw both enantiomers (just write if it exists an enantiomer). BE CAREFUL TO SHOW THE CORRECT ORIENTATION, AND THE CORRECT STEREOCHEMISTRY IN CASES WHERE STEREOCHEM IS FACTOR. Write also the name of the reaction that is occurring. OK Ph THE Br
Draw a reaction coordinate diagram in which the structure of the transition site is more similar to the product of the reaction than to the reactant.