Organic Functional Groups - Organic Chemistry

An amino group is a nitrogen-containing functional group, and is the part pictured on the right of the given molecule. This amine has three substituents: the alkyl ketone, the methyl, and the ethyl. Hydrogens do not count as "substituents." Any amine with three substituents is considered a "tertiary" amine.

This amine is chiral because it has four different substitutions at the nitrogen atom, which is the definition of chirality.

Note: "tetriary" is not a real term in organic chemistry.

A tertiary amine has three organic groups bonded to it. Triethylamine has three ethyl groups bonded to it, so that is the correct answer. Ammonia is , so it has no organic groups attached. Piperidine is a six-membered ring with a nitrogen as one of the members, making it a secondary amine. Aniline is a benzene ring with a bonded to it, so it is a primary amine.

C is the correct answer.

The molecule pictured above is an anime because it contains a nitrogen group bonded to two hydrogen atoms and one R-group. A shows an aldehyde, B shows an amide, and D shows a carboxylic acid.

In this question, we're shown the structure of the nucleoside called guanosine. We're asked to determine how many amide functional groups exist in this molecule.

First, to answer this question, we need to know what an amide functional group is. Amides consist of a carbon atom double bonded to an oxygen atom, and single bonded to a nitrogen atom. Note that this is distinct from the similarly named amine functional group, which contains a nitrogen atom with a lone pair of electrons and single bonded to three other atoms, which can be hydrogen or "R-groups" containing carbon atoms.

When looking at the molecular structure of guanosine, we can see that there is only a single amide group.

For this question, we're being asked to identify a characteristic of ammonia.

First, we need to remember what ammonia is. Ammonia is a molecule that consists of a nitrogen atom bonded to three separate hydrogen atoms. In doing so, these three bonds contribute to six of the valence shell electrons for nitrogen. The remaining two valence electrons exists on the nitrogen atom as a lone pair. Thus, there is only one lone pair of electrons (pair being two).

Also, the lone pair of electrons on ammonia allows it to act as a Lewis base by donating them (not a Lewis acid, which accepts electrons). Furthermore, this tendency for ammonia to donate its electrons would make it a nucleophile, not an electrophile.

The molecule's longest carbon chain has 3 carbons (thus, "prop"), and the lack of double bonds makes it an alkANe (thus "propan-"). The only functional group on this molecule is the amino group (thus "propanamine"), located on carbon number 1 if read from right to left, or carbon number 3 if read from left to right. The IUPAC rules state that the correct name for a molecule numbers the carbon chain such that functional groups get the lowest numbers possible. Thus "1-propanamine."

For a compound to be considered aromatic, it must be flat, cyclic, and conjugated and it must obey Huckel's rule. Huckel's rule states that an aromatic compound must have pi electrons in the overlapping p orbitals in order to be aromatic (n in this formula represents any integer). Only compounds with 2, 6, 10, 14, . . . pi electrons can be considered aromatic. Compound A has 6 pi electrons, compound B has 4, and compound C has 8. This eliminates answers B and C. Answer D is not cyclic, and therefore cannot be aromatic. The only aromatic compound is answer choice A, which you should recognize as benzene.

The correct answer is (8) Annulene. This is because all aromatic compounds must follow Huckel's Rule, which is 4n+2. Note that "n" in Huckel's Rule just refers to any whole number, and 4n+2 should result in the number of pi electrons an aromatic compound should have. For example, 4(0)+2 gives a two-pi-electron aromatic compound.

It is also important to note that Huckel's Rule is just one of three main rules in identifying an aromatic compound. An annulene is a system of conjugated monocyclic hydrocarbons. A compound is considered anti-aromatic if it follows the first two rules for aromaticity (1. Pi bonds are in a cyclic structure and 2. The structure must be planar), but does not follow the third rule, which is Huckel's Rule.

(8) Annulene follows the first two rules, but not Huckel's Rule, and is therefore antiaromatic; no value of a whole number for "n" will result in 8 with the formula 4n+2.

A molecule is anti-aromatic when it follows all of the criteria for an aromatic compound, except for the fact that it has pi electrons rather than pi electrons, as in this case.

A molecule is aromatic when it adheres to 4 main criteria:

1. The molecule must be planar

2. The molecule must be cyclic

3. Every atom in the aromatic ring must have a p orbital

4. The ring must contain pi electrons

The carbon on the left side of this molecule is an sp3 carbon, and therefore lacks an unhybridized p orbital. The molecule is non-aromatic.

There are 14 pi electrons because oxygen must contribute 2 pi electrons to avoid antiaromaticity. The other 12 pi electrons come from the 6 double bonds.

Nitrogen does not contribute any pi electrons, as it is hybridized and it's lone pairs are stored in sp2 orbitals, incapable of pi delocalization. Each nitrogen's p orbital is occupied by the double bond.

If oxygen contributes any pi electrons, the molecule will have 12 pi electrons, or 4n pi electrons, and become antiarmoatic. As it is now, the compound is antiaromatic.

Nitrogen cannot give any pi electrons because it's lone pair is in an sp2 orbital. Boron has no pi electrons to give, and only has an empty p orbital.

There is no p orbital surrounding the Boron atom, so the ring does not have a fully conjugated pi system. In addition, there are 8 electrons, 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.

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

In this question, we're presented with the structure of anthracene, and we're asked to find which answer choices represent a true statement about anthracene. Let's go through each of the choices and analyze them, one by one.

First, let's determine if anthracene is planar, which is essentially asking if the molecule is flat. When looking at anthracene, we see that the molecule is conjugated, meaning there are alternating single and double bonds. If we look at each of the carbons in this molecule, we see that all of them are hybridized. This means that each of the three other atoms connected to the carbon are organized at a angle in a single plane. Since ALL of the carbons are this way, we can conclude that anthracene is a planar compound.

Now let's determine the total number of pi electrons in anthracene. Remember, pi electrons are those that contribute to double and triple bonds. So, we'll need to count the number of double bonds contained in this molecule, which turns out to be . But, don't forget that for every double bond there are two pi electrons! Therefore, the total number of pi electrons is twice the amount of the number of double bonds, which gives a value of pi electrons. This is indeed an even number.

Lastly, let's see if anthracene satisfies Huckel's rule. This rule is one of the conditions that must be met for a molecule to be aromatic. It states that when the total number of pi electrons is equal to , we will be able to have be an integer value. So let's see if this works.

Since we arrived at an integer value for , we can conclude that Huckel's rule has indeed been satisfied.

All of the answer choices are true statements with regards to anthracene.

When determining whether a molecule is aromatic, it is important to understand that aromatic molecules are the most stable, followed by molecules that are non-aromatic, followed by molecules that are antiaromatic (the least stable). Therefore, if it is possible that a molecule can achieve a greater stability through switching the hybridization of one of its substituent atoms, it will do this.

An aromatic must follow four basic criteria: it must be a ring planar, have a continuous chain of unhybridized p orbitals (a series of sp2-hybridized atoms forming a conjugated system), and have an odd number of delocalized electron pairs in the system. Furan is planar ring (fulfilling criteria and , and its oxygen atom has a choice of being sp3-hybridized or sp2-hybridized. Depending on what hybridization the oxygen atom chooses will determine whether the molecule is aromatic or not.

If the oxygen is sp3-hybridized, the molecule will not have a continuous chain of unhybridized p orbitals, and will not be considered aromatic (it will be non-aromatic). If the oxygen is sp2-hybridized, it will fulfill criterion . Placing one of its lone pairs into the unhybridized p orbital will add two more electrons into the conjugated system, bringing the total number of electrons to (or, it will have pairs of electrons). Because it has an odd number of delocalized electrons it fulfills criterion , and therefore the molecule will be considered aromatic.

Because an aromatic molecule is more stable than a non-aromatic molecule, and by switching the hybridization of the oxygen atom the molecule can achieve aromaticity, a furan molecule will be considered an aromatic molecule.

An aromatic must follow four basic criteria: it must be a ring planar, have a continuous chain of unhybridized p orbitals (a series of sp2-hybridized atoms forming a conjugated system), and have an odd number of delocalized electron pairs in the system. This molecule cannot be considered aromatic because this sp3 carbon cannot switch its hybridization (it has no lone pairs). Therefore, it fails to follow criterion and is not considered an aromatic molecule. It is a non-aromatic molecule.

An aromatic must follow four basic criteria: it must be a ring planar, have a continuous chain of unhybridized p orbitals (a series of sp2-hybridized atoms forming a conjugated system), and have an odd number of delocalized electron pairs in the system. If the molecule fails any of the first three criteria, it is considered non-aromatic, and if it fails the only the fourth criterion (it has an even number of delocalized electron pairs), the molecule is considered antiaromatic. In the case of cyclobutadiene, by virtue of its structure follows criteria and . However, it violates criterion by having two (an even number) of delocalized electron pairs. Although it's possible that a molecule can try to escape from being antiaromatic by contorting its 3D shape so it is not planar, cyclobutadiene is too small to do this effectively. Therefore, cyclobutadiene is considered antiaromatic.

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