Highlight in red the primary carbons in this molecule. Highlight the tertiary carbons in blue. show work. don't give Ai generated solution OH Cl
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![Highlight in red the primary carbons in this molecule. Highlight the tertiary carbons in blue.
show work. don't
give Ai generated
solution
OH
Cl](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fc19fe703-75de-44d7-98b5-d61b8c958ad8%2F229573c4-1508-498c-872c-003bbb5ad880%2Fm18n2bv_processed.jpeg&w=3840&q=75)
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- ! (please do all if u hv plan to do only one or 3 please skip, let others do ) plz give explanation , I have posted again previous ans was wrong and no explantion givenPlease solve this question correctly. I'll upvote your work. Thank you for your time and help.Consider the product below a) Would this product show a signal in a UV-Vis spectrum? Why? b) Would this molecule have a non-zero alpha-value in polarimetry? Why? c) What stretches would be expected in an IR spectrum of this molecule? d) Predict the 1H NMR spectrum for this molecule. For H1 to H6 e) Predict the 13C NMR spectrum and DEPT spectra for Carbon A- Carbon G. Use (+) for positive signals, (-) for negative signals, and (X) for no signal in the DEPT NMR spectra. f) If a base such as NaOH was used, it would be harder to determine the major product before running the reaction. Once the reaction was run, how would you determine the product favored using spectroscopy?
- Organic Chemistry 1 Explain all of the steps clearly and logically. Do not just draw a picture. Clearly explain your answer in a step-by-step fashion. Here is the instructor's answer to the problem.help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all workingImage attached. Provide missing information?
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