Organic Chemistry : Organic Functional Groups

Study concepts, example questions & explanations for Organic Chemistry

varsity tutors app store varsity tutors android store

Example Questions

Example Question #11 :Organic Functional Groups And Molecules

Octagon

Assuming that this molecule is planar, determine whether this molecule is aromatic, and name the number ofelectrons (molecular orbitals).

Possible Answers:

Aromatic, 8electrons

Non aromatic, 6electrons

Aromatic, 6electrons

Not aromatic, 8electrons

Correct answer:

Not aromatic, 8electrons

Explanation:

There is no p orbital surrounding the Boron atom, so the ring does not have a fully conjugated pi system. In addition, there are 8electrons, which does not follow Huckel's rule (an aromatic system contains 4n+2 electrons). The pi electrons include the lone pair (not shown, but implicit) on the nitrogen atom, which is why the answers with "6 electrons" are not correct.

Example Question #12 :Organic Functional Groups And Molecules

1

Assuming that this molecule is planar, determine whether this molecule is aromatic, and name the number ofelectrons (notmolecular orbitals).

Possible Answers:

Not aromatic, 6electrons.

Aromatic, 6electrons.

Not aromatic, 8electrons.

Aromatic, 8electrons.

Correct answer:

Aromatic, 6electrons.

Explanation:

The lone pairs on the two nitrogen atoms reside in sp2 orbitals, meaning they do not participate in resonance. Within the ring, there are threebonds, meaning there are sixelectrons. Thus, the molecule is aromatic because it is planar and follows Huckel's rule.

Example Question #13 :Organic Functional Groups And Molecules

Identify the given organic functional group.

Fullsizerender-1

Possible Answers:

Ester

Ketone

Carboxylic acid

Acid anhydride

Aldehyde

Correct answer:

Aldehyde

Explanation:

Aldehydes are carbonyls with one R-group and one hydrogen attached to the carbonyl carbon.

Example Question #14 :Organic Functional Groups And Molecules

Identify the given organic functional group.

Fullsizerender-7

Possible Answers:

Ketone

Carboxylic acid

Acetal

Ester

Aldehyde

Correct answer:

Ketone

Explanation:

Ketones are carbonyls with two R-groups attached the the carbonyl carbon.

Example Question #15 :Organic Functional Groups And Molecules

Identify the given organic functional group.

Fullsizerender-3

Possible Answers:

Amide

Carboxylic acid

Ester

Acid halide

Acid anhydride

Correct answer:

Acid halide

Explanation:

This is an acid halide, were X is any halogen (group VII). They are the most reactive of all the carboxylic acid derivatives.

Example Question #16 :Organic Functional Groups And Molecules

Identify the given organic functional group.

Fullsizerender-8

Possible Answers:

Aldehyde

Acid anhydride

Ester

Carboxylic acid

Ketone

Correct answer:

Carboxylic acid

Explanation:

Carboxylic acids are composed of one R goup and a hydroxy group bound to the carbonyl carbon. The hydroxyl group gives the molecule acidic properties.

Example Question #17 :Organic Functional Groups And Molecules

Identify the given organic functional group.

Fullsizerender-5

Possible Answers:

Aldehyde

Acid anhydride

Acetal

Hemiketal

Ester

Correct answer:

Hemiketal

Explanation:

This is a hemiketal. Hemiketals are formed from the reaction of a ketone with an alcohol. The alcohol attacks the carbonyl carbon, reducing the double bond and adding a hydroxyl group.

Example Question #18 :Organic Functional Groups And Molecules

Identify the given organic functional group.

Fullsizerender-4

Possible Answers:

Ketal

Hemiketal

Hemiacetal

Acetal

Acid anhydride

Correct answer:

Ketal

Explanation:

Ketals have two -OR groups bound to a central carbon. The R groups attached to the oxygens are not necessarily the same. Ketals result from the reaction of a ketone with two equivalents of alcohol.

Example Question #1 :Identifying Carbonyl Compounds

Identify the given organic functional group.

Fullsizerender

Possible Answers:

Carboxylic acid

Acid anhydride

Ester

Hemiacetal

Acetal

Correct answer:

Acid anhydride

Explanation:

Acid anhydrides are relatively reactive, since they have a fairly good leaving group (the conjugate base of a carboxylic acid) [COO-]. They are formed by reacting two carboxylic acids via dehydration synthesis.

Example Question #20 :Organic Functional Groups And Molecules

Identify the given organic functional group.

Fullsizerender-2

Possible Answers:

Amide

Amine

Ester

Imine

Correct answer:

Amide

Explanation:

This is an amide. It is very unreactive since its leaving group is the conjugate base of an amine [HNR-].

Learning Tools by Varsity Tutors