
Which of the following does not give the iodoform test?
A. ${{\text{C}}_{2}}{{\text{H}}_{5}}\text{OH}$
B. ${{\text{C}}_{6}}{{\text{H}}_{5}}\text{OH}$
C. ${{\text{(C}{{\text{H}}_{3}}\text{)}}_{2}}\text{CHOH}$
D. All of the above
Answer
512.1k+ views
Hint: Iodoform test is used to test whether the carbonyl group or alcohol group is present or not in the molecule. The compound with ketone and alcohol groups will give a positive test for the iodoform. Iodine along with a base is used as a reactant.
Complete answer:
- In the given question, we have to identify the molecule which will not give the positive test for iodine.
- Iodoform test is used to identify the presence of a carbonyl such as \[\text{R - CO - C}{{\text{H}}_{3}}\text{ }\] or alcohol group such as \[\text{R - CH(OH)-}\].
- When iodine, a base such as sodium hydroxide is combined with the compound containing methyl ketone or secondary alcohol which has a methyl group.
- Then they form a precipitate of yellow coloured triiodomethane which confirms the presence of the carbonyl group.
- With ethyl alcohol:
\[\text{C}{{\text{H}}_{3}}\text{CHOH + }{{\text{I}}_{2}}\text{ + NaOH }\to \text{ CH}{{\text{I}}_{3}}\text{ + COONa}\]
- With ${{\text{(C}{{\text{H}}_{3}}\text{)}}_{2}}\text{CHOH}$
\[{{(\text{C}{{\text{H}}_{3}})}_{2}}\text{CHOH + }{{\text{I}}_{2}}\text{ }+\text{ NaOH }\to \text{ CH}{{\text{I}}_{3}}+\text{ C}{{\text{H}}_{3}}\text{COONa}\]
- whereas not only ketogenic or alcoholic groups but the aldehyde such as acetaldehyde can also give the positive iodoform test because it consists of a methyl group attached to the carbonyl, \[\text{C}{{\text{H}}_{3}}\text{ - C=O}\].
- So, among the given options only option B will not give the positive iodoform test because there is no presence of the methyl group in the molecule.
- Whereas in option A and B, a methyl group is present as we can see
\[\text{C}{{\text{H}}_{3}}\text{CHOH and C}{{\text{H}}_{3}}\text{C = O}\].
Therefore, option B is the correct answer.
Note:
As we know that iodine has antiseptic properties. So, in ancient times the iodoform was used as a disinfectant to kill the bacteria and an antiseptic to heal the wounds. Moreover, iodoform has a saffron-like structure with hexagonal structure.
Complete answer:
- In the given question, we have to identify the molecule which will not give the positive test for iodine.
- Iodoform test is used to identify the presence of a carbonyl such as \[\text{R - CO - C}{{\text{H}}_{3}}\text{ }\] or alcohol group such as \[\text{R - CH(OH)-}\].
- When iodine, a base such as sodium hydroxide is combined with the compound containing methyl ketone or secondary alcohol which has a methyl group.
- Then they form a precipitate of yellow coloured triiodomethane which confirms the presence of the carbonyl group.
- With ethyl alcohol:
\[\text{C}{{\text{H}}_{3}}\text{CHOH + }{{\text{I}}_{2}}\text{ + NaOH }\to \text{ CH}{{\text{I}}_{3}}\text{ + COONa}\]
- With ${{\text{(C}{{\text{H}}_{3}}\text{)}}_{2}}\text{CHOH}$
\[{{(\text{C}{{\text{H}}_{3}})}_{2}}\text{CHOH + }{{\text{I}}_{2}}\text{ }+\text{ NaOH }\to \text{ CH}{{\text{I}}_{3}}+\text{ C}{{\text{H}}_{3}}\text{COONa}\]
- whereas not only ketogenic or alcoholic groups but the aldehyde such as acetaldehyde can also give the positive iodoform test because it consists of a methyl group attached to the carbonyl, \[\text{C}{{\text{H}}_{3}}\text{ - C=O}\].
- So, among the given options only option B will not give the positive iodoform test because there is no presence of the methyl group in the molecule.
- Whereas in option A and B, a methyl group is present as we can see
\[\text{C}{{\text{H}}_{3}}\text{CHOH and C}{{\text{H}}_{3}}\text{C = O}\].
Therefore, option B is the correct answer.
Note:
As we know that iodine has antiseptic properties. So, in ancient times the iodoform was used as a disinfectant to kill the bacteria and an antiseptic to heal the wounds. Moreover, iodoform has a saffron-like structure with hexagonal structure.
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