Example: For the synthesis of adipic acid from cyclohexanone, 1.0 mL of nitric acid and 0.154 g of cyclohexanone were used initially. Following the reaction, 0.325 g of crude product was isolated as light yellow clumps, with a mp range of 145-150 °C. This crude product was purified by recrystallization to yield 0.173 g of pure product (off-white crystals), with a mp range of 151-153 °C. A typical yield of adipic acid is 0.190 g. Use the space provided to write out the Results and Discussion sections that would appear in a lab report for this experiment. 8 1.0nL 0.1540 0.3259 HNO, 145-150°C COOH COOH C 0.1739 151-15342

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Example: For the synthesis of adipic acid from cyclohexanone, 1.0 mL of nitric acid and
0.154 g of cyclohexanone were used initially. Following the reaction, 0.325 g of crude
product was isolated as light yellow clumps, with a mp range of 145-150 °C. This crude
product was purified by recrystallization to yield 0.173 g of pure product (off-white
crystals), with a mp range of 151-153 °C. A typical yield of adipic acid is 0.190 g. Use the
space provided to write out the Results and Discussion sections that would appear in a
lab report for this experiment.
0.15401.0L
Cyclohexanone
0.3259
HNO,
145-150°C
COOH
COOH
0.1739
151-1534
Adipic acid
Transcribed Image Text:Example: For the synthesis of adipic acid from cyclohexanone, 1.0 mL of nitric acid and 0.154 g of cyclohexanone were used initially. Following the reaction, 0.325 g of crude product was isolated as light yellow clumps, with a mp range of 145-150 °C. This crude product was purified by recrystallization to yield 0.173 g of pure product (off-white crystals), with a mp range of 151-153 °C. A typical yield of adipic acid is 0.190 g. Use the space provided to write out the Results and Discussion sections that would appear in a lab report for this experiment. 0.15401.0L Cyclohexanone 0.3259 HNO, 145-150°C COOH COOH 0.1739 151-1534 Adipic acid
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