[유기화학실험 A+] Acetanilide to p-Nitroaniline (prelab/프리랩/예비보고서)
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- 2023.09.26
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- 2022.11
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"[유기화학실험 A+] Acetanilide to p-Nitroaniline (prelab/프리랩/예비보고서)"에 대한 내용입니다.
목차
1. Objectives
2. Principles & Methods
3. References
본문내용
Objectives: The goal of this experiment is to synthesize p-nitroaniline by using aromatic nitration and hydrolysis.
Principles & Methods
(1) Principles:
Disubstituted benzenes are named using the prefixes ortho-, meta- and para-. “ortho-” is named to the form of two substituents bonded to the nearest carbon of the aromatic ring. “meta” is named when two substituents of the compound are bounded to a position where one carbon has been skipped. “para-“ is named to a compound which two substituents locate at the opposite end of the aromatic ring.
참고 자료
John A. Landgrebe. “Theory and Practice in the Organic Laboratory” 5th ed. 2005. Thomson Wadsworth.
Leory G. and Jan William Simek. “Organic Chemistry” 2017 Pearson. 849-850p.
https://pubchem.ncbi.nlm.nih.gov/
wikipedia (“4-nitroaniline”, “nitration”, “hydrolysis”)
https://labmonk.com/synthesis-of-p-nitroaniline-from-acetanilide