Draw structural formulas for the two compounds you could use to prepare the amine shown by reductive amination.HYou do not have to consider stereochemistry.• Do not include the reducing agent in your answer.If there is more than one combination, draw only one.• Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.• Separate multiple reactants using the + sign from the drop-down menu.ChemDoodle®▾n[>

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Answered: Draw structural formulas for the two…

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter21: Benzene And The Concept Of Aromaticity

Section: Chapter Questions

Problem 21.63P

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A student was trying to determine the identity of an unknown compound. The melting point of the compound was 117-118oC. The student narrowed the possible compound down to the following: Compound Melting Point Range acetanilide 113-115oC fluorene 114-116oC mandelic acid 120-122oC A second student, doing the same experiment as above, found that their melting point was 100-108oC. What is wrong with the student’s melting point? Propose two reasons why the melting point could be incorrect. View keyboard shortcuts
3. The Ninhydrin test is originally intended for what class of biomolecules? Why do have similar reactions with amines?
For the structure shown at the right, what type of compound is it? A. an ylide B. a nitrile C. a cyanohydrin D. an imine E. None of the selections are correct
Select two substrates and one reagent from each of the given pools to create the amine target molecule.
A student was trying to determine the identity of an unknown compound. The melting point of the compound was 117-118oC. The student narrowed the possible compound down to the following: Compound Melting Point Range acetanilide 113-115oC fluorene 114-116oC mandelic acid 120-122oC Explain in detail how the student can experimentally determine and confirm the identity of their unknown.
3. You are given a mixture of aspirin, phenol, and naphthalene that you need to separate. i) Draw the structures of each, and identify if they are acidic, basic, or neutral compounds. For each compound draw their reaction with the appropriate acidic or basic conditions that will change their solubility and allow them to be separated. ii) What modifications would you have to make to the experimental protocol in order to separate these three compounds? Provide specifics.
Please answer Ture or False with full explanation 7. Ethanol is a glutamate agonist. 8. Withdrawal from ethanol is safer than withdrawal from heroin. 9. Detoxifying from ethanol can cause seizures. 10. Unlike cocaine and heroin, THC is not consistently reinforcing for laboratory rodents. 11. Endocannabinoids are released primarily from terminal boutons under the influence of action potentials.
Draw the product that will form if the amine in Figure 25 reacts with hydrochloric acid in an acid-based reaction.
Think about the chemical reactions in which the H⁺-ion is involved. In how many positions can this ion bond to lovastatin in Figure 1? * A- 9 B- 7 C- 5 D- 3 E- 1
Please answer all with short explanation otherwise don't attempt Chemistry TRUE or FALSE 1. The conjugate acid form of a drug has a higher dissolution than the salt form. 2. The stable form of a solid drug has a lower solubility and dissolution than the metastable form. 3. The larger the particle size, the smaller the surface area. 4. Generally, the lower the temperature, the higher the dissolution 5. Hydrates have better dissolution than anhydrous forms. 6. The lower the volume of the solvent, the better the dissolution. 7. The larger the surface area, the higher the dissolution.
Which one will result to acidification in Hinsberg's test?2,2-Dimethylbutylamine, 2-Ethylbutylamine, N,N-dimethyl isobutylamine, methyl(2-methylbutyl)amine
Which form of amphetamine would you expect to be present at pH 1.0?

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