How do I do this whole problem?
1 answer:
The solubility of a substance in water is dependent on the temperature. Thus for
1 & 2: Temperature is the independent variable (the one that changes in the first place) and Solubility is a dependent variable (a variable that changes in response to changes in the independent variable.)
The graph: by convention you shall label the horizontal axis with the independent variable and the vertical axis with the dependent variable. For clarity's sake you shall use the finest scale possible that accommodates for all data provided for both axis. Plot the data points on the graph as if they are points on a cartesian plane.
My teacher made no detailed requirements on the phrasing on titles of solubility curve plots; however, like most other graphs in chemistry, the title shall specify the name of variables presented in this visualization. For instance, "the solubility of under different temperatures" might do. You shall refer to your textbooks for such convention.
It is necessary to interpolate to find the solubility at a temperature not given in the table. Start by connecting all given data points with a smooth line; find the vertical line corresponding to temperature = 75 degree Celsius and determine the solubility at the intersection of the vertical line and the trend line. That point shall approximates the solubility of the salt at that temperature.
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The reducing agent can approach the carbonyl face of camphor by forming a one carbon bridge (known as an exo attack) or a two carbon bridge (termed endo).
The two resultant stereoisomers are known as isoborneol and borneol (from exo attack) (from endo attack). Gas chromatography (GC) analysis may be used to calculate the ratio of each isomeric alcohol in the mixture. Unfortunately, IR analysis does not permit this.
The stereochemistry of the reaction is regulated in stiff cyclic compounds like camphor and norcamphor by protecting one side of the carbonyl group from the reagent's assault. The hydrogen atom is added to the endo side, creating the exo alcohol isoborneol, while the methyl groups on the one-carbon bridge of camphor screen the approach of the hydride from the "top" or exo side of the two-carbon bridge. You will be asked to guess the main isomeric alcohol created by the norcamphor hydride reduction later in the lab report.
To view more about rational reaction, refer to:
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