5. Results and Discussions
5.1 Methyl erucate synthesis
5.1.1 Chemical analysis of erucic acid
Physicochemical properties of erucic acid used for the synthesis of sucrose erucate were analyzed. The results of analysis are depicted in Table 5.1
Table 5.1 Analysis of erucic acid
Acid value 166.03 ± 0.9 mg KOH/gm
Iodine value 78.04 ± 1.2 g I2/100gm
Saponification value 168.05 ± 0.8 mg KOH/gm
5.1.2 Analysis of methyl erucate
After synthesis and purification of synthesized methyl erucate general characteristics of product were tested. The results obtained are shown in Table 5.2 and Figure 5.1 Figure 5.1 Color of methyl erucate
Table 5.2 General characteristics of methyl erucate
Color Light yellow
Odour
Consistency
The results of chemical analysis
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Figure 5.2 TLC of methyl erucate [Solvent: chloroform: hexane (1:1)]
Rf value = (Distance travelled by solute )/(Distance travelled by solvent front)
=
5.1.5 Spectroscopy analysis using Fourier Transform Infrared Spectroscopy (FTIR)
The infrared spectra of the purified methyl erucate showed the characteristics band at 1739 cm-1 which attributed to carbonyl ester band (Figure 5.3). The other absorptions attributed to the molecule are shown in Table 5.4. Also the IR absorption peak can be compared as shown in Figure 5.3 and Figure 5.4.
Table 5.4 Spectroscopic identification of erucic acid functional groups in FTIR
Absorption frequency range(cm-1) Absorption peak (cm-1) Type of vibration
3020-3100 2920 =C-H stretch of alkene
2850-3000 2852 C-H stretch of alkane
1705-1720 1710 C=O stretch of acid
1350-1480 1452 -CH bend of alkane
1210-1320 1284 C-O stretch of acid
675-1000 931 =C-H bend of alkene
720-725 721 C-H rock of alkane
Figure 5.3 FTIR spectra of erucic
As different bonds require different amounts of energy to bend and stretch, they absorb and transmit different amounts of radiation. This data is then collected by the spectrometer and transposed into graph form. The different amounts of absorbance for various functional groups and types of bonds have been established and can be used to identify compounds. Also, an IR spectrum can be compared to known “fingerprint” spectra in order to identify the compound. When compared to the fingerprint spectrum for 1-bromobutane found in Experimental Organic Chemistry, the IR spectrum collected from the data was very similar.
This Rf value is the higher among the other compounds because the Rf values decreases from aspirin to caffeine; therefore, this suggests that the
Bromination of (E)-Stilbene Kaisha Butz Lab Partner: Jenna Knafo Instructor: Dr. Beatrix Aukszi LA: Paige Swalley 10/28/2014 Abstract: The purpose of this experiment was to synthesize the second intermediate (meso-stilbene dibromide) in the E-Stilbene reaction by Bromination. It was hypothesized that if the reaction was heated at 120°C for five minutes the reaction between E-stilbene and the pyridium bromide perbromide would occur, and meso-stilbene would be created. After the reaction occurred the results were analyzed by IR and by an ignition test.
Based on this lab, FTIR spectroscopy affirmed functional groups present in Unknown 30A because it revealed specific transmittance bands for those functional
When the aqueous layer was added to the vial, calcium chloride was then added to dry the solution. If the solution was dry enough, a large peak between 3300-3500 would have been present in the IR spectrum. In order to obtain the IR spectrum two Classification test were performed. The Bromine test and Permanganate test were used to determine if alkenes were indeed present in the solution. Both test were positive for the compound.
A control was used to compare the reactant and the product, showing a clear appearance that would indicate an alkene being present. Bromine was added to the reactant 4-methylcyclohexanol, and a reddish-brown color appeared, indicating that no reaction took place. Bromine was then added to the product 4-methylcyclohexene, and the clear appearance of the product remained, concluding that an alkene is indeed present. Discussion Given the results obtained post-experiment, the percent yield was calculated to be about 35.5%, which may suggest that either product was lost at some point during the experiment, or side product was formed.
Lastly, product was GC traced to obtain the percentage of product and starting material within final product. Observations: Mixture turned yellow as sulfuric acid was added. During reflux condensation, sodium bromide dissolved and brown layer formed on top of solution as it boiled. Brown layer was alkyl bromide while clear, bottom layer was inorganic salts. After simple distillation, product was clear and colorless.
If the water has been dispensed into another container, this reaction would have continuously run toward to the products side. Following the isolation of the ester, a drop of Isopentyl Acetate was placed into an infrared spectrometer. When bonds within molecules absorb photons at different frequencies the IR spectrometer produces a graph to represent the bonds within the ester
Identification of Unknown Solutions and Ammonium Salts preAice Chemistry Lab Report Descriptions of unknown solutions: Unknown Descriptions A Clear, colorless, odorless liquid. B Clear, colorless, odorless liquid. C Clear, red-brown, odorless liquid D Clear, yellow-orange, odorless liquid.
Discussion This experiment done in lab was the Bromination of (E)-Stilbene to produce dibromide stilbene. Though there are three products, the meso-stilbene product is the major product. In order to get theunderstand how to get the correct major product, the full mechanism must be done.
The purpose of this experiment was to identify the two components of an unknown mixture through diverse experimental techniques such as recrystallization, extraction, melting point, and acid-base reactions. From this, the group to which these two compounds belong to had to be determined. These groups are: Carboxylic Acids, phenols, and neutrals. By determining the melting points of the two unknown compounds, these values were compared to the values of melting points in the chart and the proper compound was selected. For the case of this experiment, the unknown mixture contained, 4-methylbenzoic acid.
My essay will determine if a local chemical manufacturing plant is in compliance with OSHA Methylene Chloride, specializing in paint stripper for the DOD. Occupational health standard establishes requirements for employers to control occupational exposure to methylene chloride. Exposure may occur through inhalation, by absorption through the skin, or through contact with the skin. The standard requires that the employer establish a regulated area where exposure to airborne concentrations of methylene chloride exceeds or can be expected to exceed either the PEL or the STEL. Determine if the plant is using a soy-based stripper that do not contain methylene chloride, N-methylpyrrolidone, or other toxic solvents, when it comes to paint stripping
The observed emission data for the different elements did not look how they were supposed to. However the “peaks” for Hydrogen were found to be 534.52 and 631.24, 534.70 and 569.11 for Helium and 529.73 and 630.71 for Mercury. The Rydberg’s Constant found to 1.1x107 8.5x104 while the known constant is 10967758.34m-1. The percent error of 0.29% and the accuracy of this reading is 99.7. The slope and intercept of the linear regression line is -0.01 3.3x10-5 and 0.02x10-1 1.9x10-6 respectfully.
Abstract – Methyl trans-cinnamate is an ester that contributes to the aroma of strawberry. It can be synthesized by an acid-catalyzed Fischer esterification of a methanol and trans-cinnamic acid under reflux. The solution was extracted to obtain the organic product, and evaporated residual solvent The yield was 68%, but there is some conflicting data regarding the purity. The melting point, IR, GC-MS indicate a highly pure desired product whereas 1H NMR shows there are unreacted reagents still present.
Industries that utilize ester compounds are the perfume industry and the flavoring industry for the smells that we smell while we wear perfume and eat things, respectively. Also glass industries use polyesters (like polymethyl acrylate, etcetera) to make glass. In the process of synthesizing an ester, it is important to include a strong acid. The concentrated acid in this experiment was sulfuric acid.