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Which of the following is NOT a proper IUPAC name?


A) 1-cyclopentanone
B) 1-pentanone
C) 2-pentanone
D) 3-pentanone

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What is the consequence of the ability of aldehydes and ketones to form hydrogen bonds?


A) They are both highly colored when in the solid state.
B) They both have boiling points less than the comparable weight alcohol.
C) They prefer to hydrogen bond molecules of the same formula and will not dissolve well in water.
D) There is more than one correct response.

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What is the major difference between a cyclic hemiacetal and a cyclic acetal?


A) The cyclic hemiacetal is an alcohol,whereas the cyclic acetal is an ether.
B) The cyclic hemiacetal is an acid,and the cyclic acetal is a base.
C) The cyclic hemiacetal contains more carbons in the ring than the cyclic acetal.
D) All of the responses are correct.

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What is the IUPAC name for the following compound? What is the IUPAC name for the following compound?   A)  3-bromobutanal B)  2-bromobutanal C)  3-bromobutanone D)  2-bromobutanone


A) 3-bromobutanal
B) 2-bromobutanal
C) 3-bromobutanone
D) 2-bromobutanone

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Which of the following products is formed when hydrogen is reacted with 3-methyl-2-butanone?


A) primary alcohol
B) secondary alcohol
C) tertiary alcohol
D) acetal

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It is not possible to produce either an aldehyde or ketone from a tertiary alcohol.

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Aldehydes and ketones would always have a higher boiling point than the corresponding hydrocarbon with the same number of carbon atoms.

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What is the IUPAC name for compound shown below? What is the IUPAC name for compound shown below?   A)  methylbutanone B)  2-methylcyclobutanone C)  1-methylcyclobutanal D)  1-methylcyclobutanone


A) methylbutanone
B) 2-methylcyclobutanone
C) 1-methylcyclobutanal
D) 1-methylcyclobutanone

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An aldehyde functional group must be on the end of a carbon chain.

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Which of the following is,in an injectable form,used for contraception?


A) norethynodrel
B) estrogen
C) progestin
D) testosterone

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Acetals are generally more stable than hemiacetals.

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The IUPAC name for formaldehyde is methanal.

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Predict the resultant compound class when an aldehyde is hydrogenated.


A) hemiketal
B) alcohol
C) carboxylic acid
D) no reaction

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Which of the following pure compounds can exhibit hydrogen bonding with itself?


A)
Which of the following pure compounds can exhibit hydrogen bonding with itself? A)    B)    C)    D)  none of these
B)
Which of the following pure compounds can exhibit hydrogen bonding with itself? A)    B)    C)    D)  none of these
C)
Which of the following pure compounds can exhibit hydrogen bonding with itself? A)    B)    C)    D)  none of these
D) none of these

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What is the IUPAC name for the compound shown below? What is the IUPAC name for the compound shown below?   A)  2-methyl-2-pentanone B)  2-methyl-4-pentanone C)  4-methyl-2-pentanone D)  2-methol-4-pentanol


A) 2-methyl-2-pentanone
B) 2-methyl-4-pentanone
C) 4-methyl-2-pentanone
D) 2-methol-4-pentanol

Correct Answer

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Which of the following is an ingredient in some inhalants? It has a characteristic medicinal odor.


A) citral
B) biacetal
C) menthone
D) camphor

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The intermediate product of two moles of a primary alcohol and one mole of a ketone would be a(n) ____.


A) acetal
B) ketal
C) hemiacetal
D) hemiketal

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Acetone is the common name for 2-butanone.

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Generally,only those organic compounds containing oxygen or nitrogen can hydrogen bond.

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Which of the following compounds upon hydrolysis would yield CH3CH2OH and CH3CH2CHO?


A)
Which of the following compounds upon hydrolysis would yield CH<sub>3</sub>CH<sub>2</sub>OH and CH<sub>3</sub>CH<sub>2</sub>CHO? A)    B)    C)    D)
B)
Which of the following compounds upon hydrolysis would yield CH<sub>3</sub>CH<sub>2</sub>OH and CH<sub>3</sub>CH<sub>2</sub>CHO? A)    B)    C)    D)
C)
Which of the following compounds upon hydrolysis would yield CH<sub>3</sub>CH<sub>2</sub>OH and CH<sub>3</sub>CH<sub>2</sub>CHO? A)    B)    C)    D)
D)
Which of the following compounds upon hydrolysis would yield CH<sub>3</sub>CH<sub>2</sub>OH and CH<sub>3</sub>CH<sub>2</sub>CHO? A)    B)    C)    D)

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