World Journal of Chemical Education. 2024, 12(2), 45-48
DOI: 10.12691/WJCE-12-2-1
Original Research

Incorporating Green Chemistry into Undergraduate Organic Chemistry Laboratory: Synthesis of Banana Oil

Weihua Wang1, and Prabin Rai1

1Department of Biology and Chemistry, Southern University and A&M College, Baton Rouge, LA 70813, United States

Pub. Date: April 09, 2024

Cite this paper

Weihua Wang and Prabin Rai. Incorporating Green Chemistry into Undergraduate Organic Chemistry Laboratory: Synthesis of Banana Oil. World Journal of Chemical Education. 2024; 12(2):45-48. doi: 10.12691/WJCE-12-2-1

Abstract

The traditional laboratory of synthesis of banana oil via Fisher esterification was modified to provide a practical integration of green chemistry concepts and principles into undergraduate organic chemistry laboratory at Southern University and A&M College-Baton Rouge campus (SUBR). Besides the traditional method described in our laboratory manual, two more modified methods for the synthesis of banana oil were added. Six out of the 12 principles of green chemistry were introduced. This laboratory offered students an opportunity to do a comparative study of the greenness and efficiency of different synthetic methods for the synthesis of banana oil and practice applying green chemistry principles into organic synthesis. The modified method II was found to be the greenest and most efficient synthetic method with least waste produced, highest atom economy and yield, environmentally benign chemicals, reduced hazardous risk, improved energy efficiency and enhanced accident prevention. Calculations of E-factor and percent atom economy were introduced. The comparison of experimental percent atom economy and percent yield was also included.

Keywords

green chemistry, organic chemistry laboratory, banana oil, Fisher Esterification, organic synthesis

Copyright

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References

[1]  Tundo, P., and Griguol, E., “Green chemistry for sustainable development,” Chem. Int., 2018, 40 (1), 18−24.
 
[2]  Anastas, P. T., and Warner, J. C, Green Chemistry: Theory and Practice; Oxford University Press, New York, 1998.
 
[3]  Bodner, G. M., “2. The quadruple bottom line: the advantages of incorporating Green Chemistry into the undergraduate chemistry major”. Green Chemical Processes: Developments in Research and Education, edited by Mark Anthony Benvenuto, Berlin, Boston: De Gruyter, 2017, pp. 7-28.
 
[4]  O’Neil, N. J., Scott, S., Relph, R., and Ponnusamy, E., “Approaches to incorporating green chemistry and safety into laboratory culture,” J. Chem. Educ., 2021, 98, 84-91.
 
[5]  Beyond Benign, Green Chemistry Commitment, https:// www.beyondbenign.org/he-whos-committed/.
 
[6]  Zare, M., Golmakani, M. T., and Niakousari, M., “Lipase synthesis of isoamyl acetate using different acyl donors: comparison of novel esterification techniques,” Lebensm. Wiss. Technol., 2019, 101, 214–219.
 
[7]  Azudin, N. Y., Sangaran, S., and Shukor, S. R. A., “Non-enzymatic synthesis route for production of isoamyl acetate in a solvent-free system using miniaturized intensified reactor,” J. Environ. Chem. Eng., 2020, 8, 103186.
 
[8]  Li, Z. Y., Tao, H. Y., and Yang, R. Z., “Preparation of isoamyl acetate by reaction-distillation using ionic liquid as catalyst,” Adv. Mater. Res. 2012, 550–553, 164–169.
 
[9]  Burton, S., and Claville, M. Catalyst: General Organic Chemistry Laboratory 220&221, Southern University and A&M College.
 
[10]  Harmer, M. A. Industrial Processes Using Solid Acid Catalysts, in Handbook of Green Chemistry and Technology; J. H. Clark, D. J. Macquarris, eds.; Blackwell Publishers London., 2002.
 
[11]  Pande, M. A., and Samant S. D. “Amberlyst-15 catalyzed acetylation of phenols and alcohols under solvent free conditions,” Recyclable Catalysis, 2012, 1, 6-9.
 
[12]  Pal, R., Sarkar, T., and Khasnobis, S., “Amberlyst-15 in organic synthesis,” ARKIVOC. 2012, (i) 570-609.
 
[13]  Sheldon, R. A., “The E factor: fifteen years on,” Green Chem., 2007, 9, 1273-1283.