if I have the following reactants: •Pyridine (fresh bottle, still with its seal unbroken, distilled and stored under nitrogen) • Piperidine (fresh bottle, still with its seal unbroken, distilled and stored under nitrogen) • Glacial acetic acid (concentrated acetic acid) • distilled water • concentrated hydrochloric acid • ethanol • trifluoroacetic acid • trifluoroacetic anhydride
if I have the following reactants: •Pyridine (fresh bottle, still with its seal unbroken, distilled and stored under nitrogen) • Piperidine (fresh bottle, still with its seal unbroken, distilled and stored under nitrogen) • Glacial acetic acid (concentrated acetic acid) • distilled water • concentrated hydrochloric acid • ethanol • trifluoroacetic acid • trifluoroacetic anhydride
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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if I have the following reactants:
•Pyridine (fresh bottle, still with its seal unbroken, distilled and stored under nitrogen)
• Piperidine (fresh bottle, still with its seal unbroken, distilled and stored under nitrogen)
• Glacial acetic acid (concentrated acetic acid)
• distilled water
• concentrated hydrochloric acid
• ethanol
• trifluoroacetic acid
• trifluoroacetic anhydride
![### Preparation of Chemical Compounds
#### Instructions: Provide a detailed method for preparing the following compounds:
**A)**
\[ \text{CH}_3\text{CH}_2\text{OCOCH}_3 \]
**B)**
\[ \begin{array}{c}
\includegraphics[height=50pt]{cyclohexylamine} \\
\text{Hexahydro-1H-azepinium ion}
\end{array} + CF_3CO_2^-\]
**C)**
\[ \text{Cyclohexylcarbonylurea} \]
\[ \begin{array}{c}
\includegraphics[height=50pt]{cyclohexylisocyanate} \\
N-(trifluoroacetyl)-1-piperidine carboxamide
\end{array} \]
### Additional Information:
- Another product may be produced along with this molecule.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F5cf437dc-af80-404d-8013-877ac047e694%2F9a66bf39-b1d8-4713-bb81-4347e7b79b40%2Fn5h42y_processed.jpeg&w=3840&q=75)
Transcribed Image Text:### Preparation of Chemical Compounds
#### Instructions: Provide a detailed method for preparing the following compounds:
**A)**
\[ \text{CH}_3\text{CH}_2\text{OCOCH}_3 \]
**B)**
\[ \begin{array}{c}
\includegraphics[height=50pt]{cyclohexylamine} \\
\text{Hexahydro-1H-azepinium ion}
\end{array} + CF_3CO_2^-\]
**C)**
\[ \text{Cyclohexylcarbonylurea} \]
\[ \begin{array}{c}
\includegraphics[height=50pt]{cyclohexylisocyanate} \\
N-(trifluoroacetyl)-1-piperidine carboxamide
\end{array} \]
### Additional Information:
- Another product may be produced along with this molecule.
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