From the reaction, only 0.654 g (68.34 % yield) of isopentyl acetate was obtained. Different factors could affect the decreasing of the percent yield. During the extractions of the aqueous layer, it was possible that some of the desired product was extracted with the aqueous layer. In addition, some product remained in the drying column when the organic layer was passed through it. Finally, it was possible that final product evaporated because the hot plate was above 80°C. Even though some mass was lost during the process, the IR spectrum showed that reaction when to completion because it showed the absence of the starting material. There was no O-H peak around 3650-3200 which is part of the starting material. Indeed, the IR spectrum showed a peak at 1738.28cm-1 which shows the presence of the final product (Isopentyl acetate). In addition, the IR showed peaks
From the reaction, only 0.654 g (68.34 % yield) of isopentyl acetate was obtained. Different factors could affect the decreasing of the percent yield. During the extractions of the aqueous layer, it was possible that some of the desired product was extracted with the aqueous layer. In addition, some product remained in the drying column when the organic layer was passed through it. Finally, it was possible that final product evaporated because the hot plate was above 80°C. Even though some mass was lost during the process, the IR spectrum showed that reaction when to completion because it showed the absence of the starting material. There was no O-H peak around 3650-3200 which is part of the starting material. Indeed, the IR spectrum showed a peak at 1738.28cm-1 which shows the presence of the final product (Isopentyl acetate). In addition, the IR showed peaks