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8. If you added the following to water what would happen to the pH of the solution. Would
become acidic, basic, or stay neutral) (6 points) a. ethanol b. phenol 9. If a compound gave a
yellow precipitate with 2,4-dinitropenyl hydrazine but did not react with Tollens reagent or turn
chromic acid green would the compound be (a) a tertiary alcohol (b) aldehyde (c) ketone 10.
Give two test that you could use to determine if a compound is an aldehyde or a ketone. 6 points)
11. Dichloromethane's density is 1.37 g/mL. Would it be the upper of lower layer in extraction
of a water solution? (6 points) 12. Calculate your theoretical yield of aspirin from 10 grams of
salicylic acid using the following equation: (8 points) -X 180 g aspirin =-g aspirin 10 g salicylic
acid X 1 mole 138 g salicylic acid1 mole 13. If your 10 grams of salicylic acid produced 11.1
grams of product, what would be the percent yield of your reaction? (8 points)
Solution
ans 8
Ethanol's hydroxyl group causes the molecule to be slightly basic
phenol in water is acidic.
ans 9 compound is a ketone
Aldehydes and ketones both react with 2,4-dinitrophenylhydrazine as a test for the carbon-
oxygen double bond to give yellow precipitate.
Tollens' test, is used to distinguish between an aldehyde and a ketone.An aldehydes is readily
oxidized, whereas ketones are not .
ans 10
Fehling's Test
Equal volumes of Fehling's A and Fehling's B are mixed and the sample is added. The resulting
solution is heated.
Aldehyde - The aldehyde is oxidised and a brick red Cu(I) oxide precipitates out,
Ketone - No reaction occurs.
Tollen's Test
This test contains the complex [Ag(NH3)2]+. It is made by mixing ammonia with silver nitrate.
Aldehyde - Upon heating with Tollen's reagent solid silver metal is produced as Ag+ is reduced
to Ag.
Ketone - No reaction occurs.
ans 11
as dichloromethane is denser than water it will form lower layer and water will form upper layer
ans 12
13.04 g
ans 13
percent yield = (actual yield/theoretical yield) x 100%
= (11.1/13.04)*100
= 85.12%

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8. If you added the following to water what would happen to the pH of.pdf

  • 1. 8. If you added the following to water what would happen to the pH of the solution. Would become acidic, basic, or stay neutral) (6 points) a. ethanol b. phenol 9. If a compound gave a yellow precipitate with 2,4-dinitropenyl hydrazine but did not react with Tollens reagent or turn chromic acid green would the compound be (a) a tertiary alcohol (b) aldehyde (c) ketone 10. Give two test that you could use to determine if a compound is an aldehyde or a ketone. 6 points) 11. Dichloromethane's density is 1.37 g/mL. Would it be the upper of lower layer in extraction of a water solution? (6 points) 12. Calculate your theoretical yield of aspirin from 10 grams of salicylic acid using the following equation: (8 points) -X 180 g aspirin =-g aspirin 10 g salicylic acid X 1 mole 138 g salicylic acid1 mole 13. If your 10 grams of salicylic acid produced 11.1 grams of product, what would be the percent yield of your reaction? (8 points) Solution ans 8 Ethanol's hydroxyl group causes the molecule to be slightly basic phenol in water is acidic. ans 9 compound is a ketone Aldehydes and ketones both react with 2,4-dinitrophenylhydrazine as a test for the carbon- oxygen double bond to give yellow precipitate. Tollens' test, is used to distinguish between an aldehyde and a ketone.An aldehydes is readily oxidized, whereas ketones are not . ans 10 Fehling's Test Equal volumes of Fehling's A and Fehling's B are mixed and the sample is added. The resulting solution is heated. Aldehyde - The aldehyde is oxidised and a brick red Cu(I) oxide precipitates out, Ketone - No reaction occurs. Tollen's Test This test contains the complex [Ag(NH3)2]+. It is made by mixing ammonia with silver nitrate. Aldehyde - Upon heating with Tollen's reagent solid silver metal is produced as Ag+ is reduced to Ag. Ketone - No reaction occurs. ans 11 as dichloromethane is denser than water it will form lower layer and water will form upper layer ans 12 13.04 g
  • 2. ans 13 percent yield = (actual yield/theoretical yield) x 100% = (11.1/13.04)*100 = 85.12%