4-Formylbenzoic acid could be reduced using different reducing agents and could produce A and B as follows. NABH4 LIAIH4 он Product A Product B H30 H 4-formylbenzoic acid i) Draw the structures of products A and B. ii) Explain how you can confirm that the reduction of 4-formylbenzoic acid to B has taken place using IR spectroscopy.

4-Formylbenzoic acid could be reduced using different reducing agents and could produce A and B as follows. NABH4 LIAIH4 он Product A Product B H30 H 4-formylbenzoic acid i) Draw the structures of products A and B. ii) Explain how you can confirm that the reduction of 4-formylbenzoic acid to B has taken place using IR spectroscopy.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter11: Reactions Of Alkyl Halides: Nucleophilic Substitutions And Eliminations

Section11.SE: Something Extra

Problem 40AP: The following Walden cycle has been carried out. Explain the results, and indicate where Walden...

See similar textbooks

Similar questions

The following Walden cycle has been carried out. Explain the results, and indicate where Walden inversion occurs.
Below is the Wolff–Kishner reduction. Describe how the IR spectrum could be used to tell if the reaction had been successful. Provide approximate wave numbers and the corresponding functional groups for the key absorption bands and/or peaks in IR. describe from two aspects: which peak(s)-wavenumber(s) of what functional group(s) should appear/remain in the IR of the products (that is/are different from the reactants); and which peak(s)-wavenumber(s) of what functional group(s) should disappear in the IR of the products (but is/are present in the reactants).
Reaction of BrCH2CH2CH2CH2NH2 with NaH forms compound W, which gives the IR and mass spectra shown below. Propose a structure for W.
Interpret the results of the UV-vis spectra and briefly explain why the 3-phenylpropionaldehyde compound did not peak but the others did (hint: conjugated system).
Part IIDraw the structure of the synthesized product (do not include side or by products) from experiments performed in Chem 272L. How can IR spectroscopy be used to monitor the progress of each of the following reactions (if reaction went to completion and/or check the purity of the final product)? What absorptions would be observed in the IR spectrum? And if IR spectroscopy could not have been used, briefly explain why.
Answer the following questions on using IR spectroscopy to characterize the products in the synthesis ofluminol.a. Can IR be used to determine if the synthesis of the hydrazide was successful? Explain youranswer.b. IR cannot be used to determine the success of the reduction of the nitro group into an amine in Part II.Explain why not.
i need help with predicting the Ir spec for the final product i also need to make it look like the example with the table and the 1h-nmr digram i made an example of how it needs to look like the lab called Electrophilic Aromatic Substitution: Friedel-CraftsAlkylation
Part IIE. Draw the structure of the synthesized product (do not include side or by products) from experiments performed in Chem 272L. How can IR spectroscopy be used to monitor the progress of each of the following reactions (if reaction went to completion and/or check the purity of the final product)? What absorptions would be observed in the IR spectrum? And if IR spectroscopy could not have been used, briefly explain why.
Which IR spectrum is consistent with an alkene?
Give the complete mechanism using curved arrow formalism for the reaction of p-chloro benzaldehyde treated with 2 equivalents of MeOH in HCl. How many peaks would be visualized in the 1H and 13C NMR for p-chloro benzaldehyde? Thank you for the he.lp
Attached is the NMR of 1-indanone (top), 3,4 dimethoxybenzaldehyde (middle), and the product of the reaction (bottom). Based on the spectra, did the reaction work to obtain a pure, final condensation product? How do you know?
looking at this reaction (first image), The second image shows the 13C NMR spectrum of the 2-acetnaphthone which is the starting material and an 13C NMR spectrum obtained for the reaction product: Based a comparison of the two 13C NMR spectra, is product A or product B the major product of the reaction? - Explain your reasoning.