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This document is a report on an experiment to calculate the specific rotation of sucrose using a polarimeter and to observe the cleavage kinetics of sucrose with acid and enzyme catalysts. The experiment involves dissolving sucrose in water and mixing it with hydrochloric acid and monochloroacetic acid solutions in polarimeter tubes. Polarization readings are taken over time to determine the rate constants and specific rotation.
This document is a report on an experiment to calculate the specific rotation of sucrose using a polarimeter and to observe the cleavage kinetics of sucrose with acid and enzyme catalysts. The experiment involves dissolving sucrose in water and mixing it with hydrochloric acid and monochloroacetic acid solutions in polarimeter tubes. Polarization readings are taken over time to determine the rate constants and specific rotation.
This document is a report on an experiment to calculate the specific rotation of sucrose using a polarimeter and to observe the cleavage kinetics of sucrose with acid and enzyme catalysts. The experiment involves dissolving sucrose in water and mixing it with hydrochloric acid and monochloroacetic acid solutions in polarimeter tubes. Polarization readings are taken over time to determine the rate constants and specific rotation.
Aim : Calculate the specific rotation of sucrose using a
Polarimeter. Observe the cleavage kinetics of sucrose with an acid catalyst, hydrochloric acid. Observe the cleavage kinetics of sucrose with an enzyme catalyst, invertase. Calculate the rate constant for each run from the rotational readings
Experimental :
Apparatus. Polarimeter (described in the Appendix); sodium-
vapor lamp; thermostat and circulating pump; two water-jacketed polarimeter tubes; two #3 rubber stoppers; pure sucrose; 100 ml of 4 M hydrochloric acid; 100 ml of 4 M monochloroacetic acid; three 25-ml pipettes.
Procedure. Twenty grams of pure cane sugar (sucrose) is
dissolved in water (filtered, if necessary, to give a clear solution) and diluted to 100 ml. The sucrose solution, the 4 M hydrochloric acid solution, and the 4 M monochloroacetic acid are placed in the 25° thermostat and allowed to stand a few minutes to come to temperature. Two jacketed polarimeter tubes are connected in series with the circulating water from a thermostat at 25° . A zero reading is taken. Twenty-five milliliters of the sucrose solution is thoroughly mixed with 25 ml of the 4 M monochloroacetic acid solution, and small portions of the solution are used to rinse out one polarimeter tube. The tube is then filled and stoppered. The second polarimeter tube is filled in a similar manner after rinsing, using 25 ml of the sugar solution and 25 ml of the 4 M hydrochloric acid solution. The tubes are filled rapidly, and readings are taken as soon as possible after mixing. The first reading is taken on the hydrochloric acid solution and recorded, and subsequent measurements are recorded about every 10 min for the first hour or so. As the reaction slows down, the observations may be taken less frequently. The observations should extend over a period of 3 hr or more. The reaction goes much more slowly with the monochloroacetic acid, and the readings are taken less frequently. Monochloroacetic acid readings are taken at convenient intervals of time when the polarimeter is not needed for the hydrochloric acid solution.