All resonance structures and the resonance hybrid for the tropylium ion and benzyl cation are to be drawn. From the resonance structures of each cation, how many structures exhibit aromaticity in the ring is to be determined. From this, the more stable cation is to be determined. Concept introduction: A curved arrow illustrates the movement of a pair of valence electrons. A curved arrow can originate from a lone pair of electrons or from the center of a covalent double or triple bond to indicate the specific pair of electrons that is being moved. The arrow points to an atom if the electrons being moved become a lone pair. Otherwise, the arrow points to the center of an existing single or double bond to represent the formation of a new double or triple bond there. When a lone pair on an atom is converted into a bonding pair, the formal charge on that atom becomes more positive by 1; when reverse happens; the formal charge on the atom becomes more negative by 1. If a species possesses a π system of MOs constructed from p atomic orbitals that are fully conjugated around a ring, then the species is: Aromatic if the number of electrons in that cyclic π system is either 2, 6, 10, 14, 18 and so on. Antiaromatic if the number of electrons in that cyclic π system is either 4, 8 , 12, 16, 20 and so on. All other species are nonaromatic.

Question

Want to see the full answer?

Answer 1

Question

Definition Definition Rule that estimates whether a given organic planar ring structure will show an aromatic property. A cyclic ring molecule is said to follow Hückel’s rule if the л-electrons count in a molecule is [4n+2], where n stands for a positive numerical value. It is also called the [4n+2] rule. Hückel's rule, sometimes referred to as the aromaticity rule, is one but not the only criteria to judge a molecule for aromaticity.

Chapter G, Problem G.4YT

Interpretation Introduction

Interpretation:

All resonance structures and the resonance hybrid for the tropylium ion and benzyl cation are to be drawn. From the resonance structures of each cation, how many structures exhibit aromaticity in the ring is to be determined. From this, the more stable cation is to be determined.

Concept introduction:

A curved arrow illustrates the movement of a pair of valence electrons. A curved arrow can originate from a lone pair of electrons or from the center of a covalent double or triple bond to indicate the specific pair of electrons that is being moved. The arrow points to an atom if the electrons being moved become a lone pair. Otherwise, the arrow points to the center of an existing single or double bond to represent the formation of a new double or triple bond there. When a lone pair on an atom is converted into a bonding pair, the formal charge on that atom becomes more positive by 1; when reverse happens; the formal charge on the atom becomes more negative by 1.

If a species possesses a π system of MOs constructed from p atomic orbitals that are fully conjugated around a ring, then the species is:

Aromatic if the number of electrons in that cyclic π system is either 2, 6, 10, 14, 18 and so on.

Antiaromatic if the number of electrons in that cyclic π system is either 4, 8, 12, 16, 20 and so on.

All other species are nonaromatic.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

The decomposition of dinitrogen pentoxide according to the equation: 50°C 2 N2O5(g) 4 NO2(g) + O2(g) follows first-order kinetics with a rate constant of 0.0065 s-1. If the initial concentration of N2O5 is 0.275 M, determine: the final concentration of N2O5 after 180 seconds. ...

Don't used hand raiting

CS2(g) →CS(g) + S(g) The rate law is Rate = k[CS2] where k = 1.6 × 10−6 s−¹. S What is the concentration of CS2 after 5 hours if the initial concentration is 0.25 M?

Answer 2

Question

Definition Definition Rule that estimates whether a given organic planar ring structure will show an aromatic property. A cyclic ring molecule is said to follow Hückel’s rule if the л-electrons count in a molecule is [4n+2], where n stands for a positive numerical value. It is also called the [4n+2] rule. Hückel's rule, sometimes referred to as the aromaticity rule, is one but not the only criteria to judge a molecule for aromaticity.

Chapter G, Problem G.4YT

Interpretation Introduction

Interpretation:

All resonance structures and the resonance hybrid for the tropylium ion and benzyl cation are to be drawn. From the resonance structures of each cation, how many structures exhibit aromaticity in the ring is to be determined. From this, the more stable cation is to be determined.

Concept introduction:

A curved arrow illustrates the movement of a pair of valence electrons. A curved arrow can originate from a lone pair of electrons or from the center of a covalent double or triple bond to indicate the specific pair of electrons that is being moved. The arrow points to an atom if the electrons being moved become a lone pair. Otherwise, the arrow points to the center of an existing single or double bond to represent the formation of a new double or triple bond there. When a lone pair on an atom is converted into a bonding pair, the formal charge on that atom becomes more positive by 1; when reverse happens; the formal charge on the atom becomes more negative by 1.

If a species possesses a π system of MOs constructed from p atomic orbitals that are fully conjugated around a ring, then the species is:

Aromatic if the number of electrons in that cyclic π system is either 2, 6, 10, 14, 18 and so on.

Antiaromatic if the number of electrons in that cyclic π system is either 4, 8, 12, 16, 20 and so on.

All other species are nonaromatic.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Definition Definition Rule that estimates whether a given organic planar ring structure will show an aromatic property. A cyclic ring molecule is said to follow Hückel’s rule if the л-electrons count in a molecule is [4n+2], where n stands for a positive numerical value. It is also called the [4n+2] rule. Hückel's rule, sometimes referred to as the aromaticity rule, is one but not the only criteria to judge a molecule for aromaticity.

Chapter G, Problem G.4YT

Interpretation Introduction

Interpretation:

All resonance structures and the resonance hybrid for the tropylium ion and benzyl cation are to be drawn. From the resonance structures of each cation, how many structures exhibit aromaticity in the ring is to be determined. From this, the more stable cation is to be determined.

Concept introduction:

A curved arrow illustrates the movement of a pair of valence electrons. A curved arrow can originate from a lone pair of electrons or from the center of a covalent double or triple bond to indicate the specific pair of electrons that is being moved. The arrow points to an atom if the electrons being moved become a lone pair. Otherwise, the arrow points to the center of an existing single or double bond to represent the formation of a new double or triple bond there. When a lone pair on an atom is converted into a bonding pair, the formal charge on that atom becomes more positive by 1; when reverse happens; the formal charge on the atom becomes more negative by 1.

If a species possesses a π system of MOs constructed from p atomic orbitals that are fully conjugated around a ring, then the species is:

Aromatic if the number of electrons in that cyclic π system is either 2, 6, 10, 14, 18 and so on.

Antiaromatic if the number of electrons in that cyclic π system is either 4, 8, 12, 16, 20 and so on.

All other species are nonaromatic.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Definition Definition Rule that estimates whether a given organic planar ring structure will show an aromatic property. A cyclic ring molecule is said to follow Hückel’s rule if the л-electrons count in a molecule is [4n+2], where n stands for a positive numerical value. It is also called the [4n+2] rule. Hückel's rule, sometimes referred to as the aromaticity rule, is one but not the only criteria to judge a molecule for aromaticity.

Chapter G, Problem G.4YT

Interpretation Introduction