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Passage Students Used Three Classification Tests to Study the Reactivity of of Alcohol

Question 74

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Students used three classification tests to study the reactivity of alcohol, aldehyde, and ketone functional groups in organic compounds.  The organic compounds provided to the students are given in Table 1.Table 1  Organic Compounds Tested
Passage Students used three classification tests to study the reactivity of alcohol, aldehyde, and ketone functional groups in organic compounds.  The organic compounds provided to the students are given in Table 1.<strong>Table 1</strong>  Organic Compounds Tested First, the students performed the Lucas test by mixing a few drops of each compound with 2 mL of the Lucas reagent (ZnCl<sub>2</sub> and HCl) .  This reagent is used to test for secondary and tertiary alcohols.  A positive test result is indicated by a cloudy reaction mixture upon addition of the Lucas reagent due to the formation of an insoluble compound by an S<sub>N</sub>1 reaction with a secondary or tertiary alcohol (Reaction 1) . <strong>Reaction 1</strong>Next, a test for alcohols and aldehydes was performed by the addition of a drop of chromic acid reagent (CrO<sub>3</sub> dissolved in aqueous H<sub>2</sub>SO<sub>4</sub>) into samples of the organic compounds.  The disappearance of the orange color from chromic acid and formation of a blue-green suspension is indicative of a positive result for this test.  Compound A was found to be an example of a positive result, as shown in Reaction 2. <strong>Reaction 2</strong>Finally, samples of the compounds were also dissolved in water, followed by the addition of NaOH and iodine.  This test is known as the iodoform test, which is used to identify methyl ketones and secondary alcohols.  A positive result is indicated by the formation of iodoform (CHI<sub>3</sub>) , a yellow precipitate (Reaction 3) . 3</strong><strong>Table 2</strong>  Selected Observations from the Classification Tests -Based on the results presented in Table 2, which compounds would give a positive result for the iodoform test?CH<sub>3</sub>CH<sub>2</sub>CHOCH<sub>3</sub>(CH<sub>2</sub>) <sub>4</sub>OHCH<sub>3</sub>(CH<sub>2</sub>) <sub>2</sub>C(O) CH<sub>3</sub>CH<sub>3</sub>(CH<sub>2</sub>) <sub>2</sub>CH(OH) CH<sub>3</sub> A) I and III only B) II and III only C) II and IV only D) III and IV only First, the students performed the Lucas test by mixing a few drops of each compound with 2 mL of the Lucas reagent (ZnCl2 and HCl) .  This reagent is used to test for secondary and tertiary alcohols.  A positive test result is indicated by a cloudy reaction mixture upon addition of the Lucas reagent due to the formation of an insoluble compound by an SN1 reaction with a secondary or tertiary alcohol (Reaction 1) .
Passage Students used three classification tests to study the reactivity of alcohol, aldehyde, and ketone functional groups in organic compounds.  The organic compounds provided to the students are given in Table 1.<strong>Table 1</strong>  Organic Compounds Tested First, the students performed the Lucas test by mixing a few drops of each compound with 2 mL of the Lucas reagent (ZnCl<sub>2</sub> and HCl) .  This reagent is used to test for secondary and tertiary alcohols.  A positive test result is indicated by a cloudy reaction mixture upon addition of the Lucas reagent due to the formation of an insoluble compound by an S<sub>N</sub>1 reaction with a secondary or tertiary alcohol (Reaction 1) . <strong>Reaction 1</strong>Next, a test for alcohols and aldehydes was performed by the addition of a drop of chromic acid reagent (CrO<sub>3</sub> dissolved in aqueous H<sub>2</sub>SO<sub>4</sub>) into samples of the organic compounds.  The disappearance of the orange color from chromic acid and formation of a blue-green suspension is indicative of a positive result for this test.  Compound A was found to be an example of a positive result, as shown in Reaction 2. <strong>Reaction 2</strong>Finally, samples of the compounds were also dissolved in water, followed by the addition of NaOH and iodine.  This test is known as the iodoform test, which is used to identify methyl ketones and secondary alcohols.  A positive result is indicated by the formation of iodoform (CHI<sub>3</sub>) , a yellow precipitate (Reaction 3) . 3</strong><strong>Table 2</strong>  Selected Observations from the Classification Tests -Based on the results presented in Table 2, which compounds would give a positive result for the iodoform test?CH<sub>3</sub>CH<sub>2</sub>CHOCH<sub>3</sub>(CH<sub>2</sub>) <sub>4</sub>OHCH<sub>3</sub>(CH<sub>2</sub>) <sub>2</sub>C(O) CH<sub>3</sub>CH<sub>3</sub>(CH<sub>2</sub>) <sub>2</sub>CH(OH) CH<sub>3</sub> A) I and III only B) II and III only C) II and IV only D) III and IV only Reaction 1Next, a test for alcohols and aldehydes was performed by the addition of a drop of chromic acid reagent (CrO3 dissolved in aqueous H2SO4) into samples of the organic compounds.  The disappearance of the orange color from chromic acid and formation of a blue-green suspension is indicative of a positive result for this test.  Compound A was found to be an example of a positive result, as shown in Reaction 2.
Passage Students used three classification tests to study the reactivity of alcohol, aldehyde, and ketone functional groups in organic compounds.  The organic compounds provided to the students are given in Table 1.<strong>Table 1</strong>  Organic Compounds Tested First, the students performed the Lucas test by mixing a few drops of each compound with 2 mL of the Lucas reagent (ZnCl<sub>2</sub> and HCl) .  This reagent is used to test for secondary and tertiary alcohols.  A positive test result is indicated by a cloudy reaction mixture upon addition of the Lucas reagent due to the formation of an insoluble compound by an S<sub>N</sub>1 reaction with a secondary or tertiary alcohol (Reaction 1) . <strong>Reaction 1</strong>Next, a test for alcohols and aldehydes was performed by the addition of a drop of chromic acid reagent (CrO<sub>3</sub> dissolved in aqueous H<sub>2</sub>SO<sub>4</sub>) into samples of the organic compounds.  The disappearance of the orange color from chromic acid and formation of a blue-green suspension is indicative of a positive result for this test.  Compound A was found to be an example of a positive result, as shown in Reaction 2. <strong>Reaction 2</strong>Finally, samples of the compounds were also dissolved in water, followed by the addition of NaOH and iodine.  This test is known as the iodoform test, which is used to identify methyl ketones and secondary alcohols.  A positive result is indicated by the formation of iodoform (CHI<sub>3</sub>) , a yellow precipitate (Reaction 3) . 3</strong><strong>Table 2</strong>  Selected Observations from the Classification Tests -Based on the results presented in Table 2, which compounds would give a positive result for the iodoform test?CH<sub>3</sub>CH<sub>2</sub>CHOCH<sub>3</sub>(CH<sub>2</sub>) <sub>4</sub>OHCH<sub>3</sub>(CH<sub>2</sub>) <sub>2</sub>C(O) CH<sub>3</sub>CH<sub>3</sub>(CH<sub>2</sub>) <sub>2</sub>CH(OH) CH<sub>3</sub> A) I and III only B) II and III only C) II and IV only D) III and IV only Reaction 2Finally, samples of the compounds were also dissolved in water, followed by the addition of NaOH and iodine.  This test is known as the iodoform test, which is used to identify methyl ketones and secondary alcohols.  A positive result is indicated by the formation of iodoform (CHI3) , a yellow precipitate (Reaction 3) .
Passage Students used three classification tests to study the reactivity of alcohol, aldehyde, and ketone functional groups in organic compounds.  The organic compounds provided to the students are given in Table 1.<strong>Table 1</strong>  Organic Compounds Tested First, the students performed the Lucas test by mixing a few drops of each compound with 2 mL of the Lucas reagent (ZnCl<sub>2</sub> and HCl) .  This reagent is used to test for secondary and tertiary alcohols.  A positive test result is indicated by a cloudy reaction mixture upon addition of the Lucas reagent due to the formation of an insoluble compound by an S<sub>N</sub>1 reaction with a secondary or tertiary alcohol (Reaction 1) . <strong>Reaction 1</strong>Next, a test for alcohols and aldehydes was performed by the addition of a drop of chromic acid reagent (CrO<sub>3</sub> dissolved in aqueous H<sub>2</sub>SO<sub>4</sub>) into samples of the organic compounds.  The disappearance of the orange color from chromic acid and formation of a blue-green suspension is indicative of a positive result for this test.  Compound A was found to be an example of a positive result, as shown in Reaction 2. <strong>Reaction 2</strong>Finally, samples of the compounds were also dissolved in water, followed by the addition of NaOH and iodine.  This test is known as the iodoform test, which is used to identify methyl ketones and secondary alcohols.  A positive result is indicated by the formation of iodoform (CHI<sub>3</sub>) , a yellow precipitate (Reaction 3) . 3</strong><strong>Table 2</strong>  Selected Observations from the Classification Tests -Based on the results presented in Table 2, which compounds would give a positive result for the iodoform test?CH<sub>3</sub>CH<sub>2</sub>CHOCH<sub>3</sub>(CH<sub>2</sub>) <sub>4</sub>OHCH<sub>3</sub>(CH<sub>2</sub>) <sub>2</sub>C(O) CH<sub>3</sub>CH<sub>3</sub>(CH<sub>2</sub>) <sub>2</sub>CH(OH) CH<sub>3</sub> A) I and III only B) II and III only C) II and IV only D) III and IV only 3Table 2  Selected Observations from the Classification Tests
Passage Students used three classification tests to study the reactivity of alcohol, aldehyde, and ketone functional groups in organic compounds.  The organic compounds provided to the students are given in Table 1.<strong>Table 1</strong>  Organic Compounds Tested First, the students performed the Lucas test by mixing a few drops of each compound with 2 mL of the Lucas reagent (ZnCl<sub>2</sub> and HCl) .  This reagent is used to test for secondary and tertiary alcohols.  A positive test result is indicated by a cloudy reaction mixture upon addition of the Lucas reagent due to the formation of an insoluble compound by an S<sub>N</sub>1 reaction with a secondary or tertiary alcohol (Reaction 1) . <strong>Reaction 1</strong>Next, a test for alcohols and aldehydes was performed by the addition of a drop of chromic acid reagent (CrO<sub>3</sub> dissolved in aqueous H<sub>2</sub>SO<sub>4</sub>) into samples of the organic compounds.  The disappearance of the orange color from chromic acid and formation of a blue-green suspension is indicative of a positive result for this test.  Compound A was found to be an example of a positive result, as shown in Reaction 2. <strong>Reaction 2</strong>Finally, samples of the compounds were also dissolved in water, followed by the addition of NaOH and iodine.  This test is known as the iodoform test, which is used to identify methyl ketones and secondary alcohols.  A positive result is indicated by the formation of iodoform (CHI<sub>3</sub>) , a yellow precipitate (Reaction 3) . 3</strong><strong>Table 2</strong>  Selected Observations from the Classification Tests -Based on the results presented in Table 2, which compounds would give a positive result for the iodoform test?CH<sub>3</sub>CH<sub>2</sub>CHOCH<sub>3</sub>(CH<sub>2</sub>) <sub>4</sub>OHCH<sub>3</sub>(CH<sub>2</sub>) <sub>2</sub>C(O) CH<sub>3</sub>CH<sub>3</sub>(CH<sub>2</sub>) <sub>2</sub>CH(OH) CH<sub>3</sub> A) I and III only B) II and III only C) II and IV only D) III and IV only
-Based on the results presented in Table 2, which compounds would give a positive result for the iodoform test?CH3CH2CHOCH3(CH2) 4OHCH3(CH2) 2C(O) CH3CH3(CH2) 2CH(OH) CH3


A) I and III only
B) II and III only
C) II and IV only
D) III and IV only

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