Question

1. How did the melting point of your acetanilide change after recrystallization? 2. Why would you...

1. How did the melting point of your acetanilide change after recrystallization?

2. Why would you test the purity of your acetanilide by mixing it with a known, pure sample of acetanilide and rechecking the m.p.?

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Answer #1

Q1.

Typically, we have a sample with acetanilide and impurities.

Recall that impurities may or may not change the melting point (MP) depending on their characteristics.

If they are non-soluble, they will not affect it. It they are soluble, they will affect, typically reducing it.

Now... we use crystallization in order to

- get rid of impurities

- increase the lattice / crystal shape of the acetanilide.

Then, most impurities are gone.

The MP will not be depressed, therefore, expect a HIGHER value of MP fo rthe pure recrystallized sample of Acetanilide.

Q2.

We would want to do this in order to compare the values of pure/impure MP as a reference.

The pure sample of an acetanilide should mark the "range" of temperature in which we should see/observe the change in color, and phase transition.

This helps so we can know the expected range, for instance, insted of waiting 1° per test, we can go directly to the desired range

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