6. Research and explain why BenadrylTM, lidocaine, and morphine are injected as Benadryl-HCI, lidocaine- HCl and morphine as morphine-sulfate.

Chemistry for Today: General, Organic, and Biochemistry
9th Edition
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Chapter16: Amines And Amides
Section: Chapter Questions
Problem 16.24E
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Need help with 6. Unsure why got rejected as this is a pre lab question and is not graded. Our lab itself is what is graded. We then follow it by post questions.
PRE-LABORATORY QUESTIONS
Complete as assigned.
1. Draw the structure of ammonia (NH3):
2. Draw the structure of methylamine:
3. Define what protonated means in terms of amines:
4. Explain why a protonated amine is water soluble:
5. Show the full structure of the salt that forms when triethylamine reacts with hydrochloric acid:
6. Research and explain why BenadrylTM, lidocaine, and morphine are injected as Benadryl-HCI, lidocaine-
HCl and morphine as morphine-sulfate.
Transcribed Image Text:PRE-LABORATORY QUESTIONS Complete as assigned. 1. Draw the structure of ammonia (NH3): 2. Draw the structure of methylamine: 3. Define what protonated means in terms of amines: 4. Explain why a protonated amine is water soluble: 5. Show the full structure of the salt that forms when triethylamine reacts with hydrochloric acid: 6. Research and explain why BenadrylTM, lidocaine, and morphine are injected as Benadryl-HCI, lidocaine- HCl and morphine as morphine-sulfate.
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