1. Compare the melting point range of your isolated N-acetylanthranilic acid with the expected melting point range and comment on the identity and purity of your product. 2. r. Show the calculation for the theoretical yield of N-acetylanthranilic acid (from the measured mass of starting material) and for the percent yield (including units). How could the percent yield be improved? 3. Did you observe fluorescence when viewing your product under a 365 nm UV lamp? What color fluorescence did you observe? What did this color fluorescence indicate about the purity of your product? Did you need to recrystallize your product? L 4. Were you able to observe the triboluminescence of your product? Describe the observed triboluminescence of your product (or of a classmate's product if your product did not display triboluminescence). What could be done to the product to increase the likelihood of observing the triboluminescence? 5. P Para-aminobenzoic acid (PABA) is an isomer of anthranilic acid that is used in sunscreen. Predict the structure of the product if PABA were to undergo a similar reaction with acetic anhydride. 요요 acetic anhydride H₂N ОН para-aminobenzoic acid 1. 2. H���O

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Complete question 2 given that the starting mass was 2.000 g anthranilic acid, theoretical yield was 2.6129 g for N-acetyl, there was 0.0146 moles in the 2.0 g anthranilic acid. Next, I found that the mass of N-acetylanthranilic acid was 1.945 grams after recrystallization

1.
Compare the melting point range of your isolated N-acetylanthranilic acid with the expected
melting point range and comment on the identity and purity of your product.
2. r.
Show the calculation for the theoretical yield of N-acetylanthranilic acid (from the measured
mass of starting material) and for the percent yield (including units). How could the percent yield be
improved?
3.
Did you observe fluorescence when viewing your product under a 365 nm UV lamp? What
color fluorescence did you observe? What did this color fluorescence indicate about the purity of your
product? Did you need to recrystallize your product?
L
4. Were you able to observe the triboluminescence of your product? Describe the observed
triboluminescence of your product (or of a classmate's product if your product did not display
triboluminescence). What could be done to the product to increase the likelihood of observing the
triboluminescence?
5. P Para-aminobenzoic acid (PABA) is an isomer of anthranilic acid that is used in sunscreen.
Predict the structure of the product if PABA were to undergo a similar reaction with acetic anhydride.
요요
acetic anhydride
H₂N
ОН
para-aminobenzoic acid
1.
2. H���O
Transcribed Image Text:1. Compare the melting point range of your isolated N-acetylanthranilic acid with the expected melting point range and comment on the identity and purity of your product. 2. r. Show the calculation for the theoretical yield of N-acetylanthranilic acid (from the measured mass of starting material) and for the percent yield (including units). How could the percent yield be improved? 3. Did you observe fluorescence when viewing your product under a 365 nm UV lamp? What color fluorescence did you observe? What did this color fluorescence indicate about the purity of your product? Did you need to recrystallize your product? L 4. Were you able to observe the triboluminescence of your product? Describe the observed triboluminescence of your product (or of a classmate's product if your product did not display triboluminescence). What could be done to the product to increase the likelihood of observing the triboluminescence? 5. P Para-aminobenzoic acid (PABA) is an isomer of anthranilic acid that is used in sunscreen. Predict the structure of the product if PABA were to undergo a similar reaction with acetic anhydride. 요요 acetic anhydride H₂N ОН para-aminobenzoic acid 1. 2. H���O
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