6. Research and explain why BenadrylTM, lidocaine, and morphine are injected as Benadryl-HCI, lidocaine- HCl and morphine as morphine-sulfate.
6. Research and explain why BenadrylTM, lidocaine, and morphine are injected as Benadryl-HCI, lidocaine- HCl and morphine as morphine-sulfate.
Chemistry
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...
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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.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb08a09d5-4e24-4c20-897d-9a1b06585eb0%2F6a2b2e02-5571-49a5-8602-3a2f8ce22e95%2Fpx25o9d_processed.jpeg&w=3840&q=75)
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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