(a) Interpretation: Each asymmetric carbon in the given molecule is to be assigned R or S configuration. Concept introduction: The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S. When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

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Answer 1

Question

Chapter C, Problem C.20P

Interpretation Introduction

(a)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(b)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(c)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(d)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

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Feedback: Your answer is incorrect. Predict the major products of the following organic reaction: CN Δ + A ? NC Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. esc Check 80 MH F1 F2 F3 F4 F5 50 @ # C % 95 € Save For Later Sub 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy C A DII F6 F7 F8 7 * 8 Λ & 6 F9 F10 9 0 4

Incorrect Feedback: Your answer is incorrect. Predict the major products of the following organic reaction: ཤིགས་བྱ རྩ་ཅད་ཀྱིས་༢༩ + Some important notes: A ^ ? • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. E Check 0 لا Save For La ©2025 McGraw Hill LLC. All Rights Reserved. Terms of All F9 A

Predict the major products of the following organic reaction: + Δ A ? Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. Explanation Check Click and drag to start drawing a structure. 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Priva

Answer 2

Question

Chapter C, Problem C.20P

Interpretation Introduction

(a)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(b)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(c)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(d)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

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Answer 3

Question

Chapter C, Problem C.20P

Interpretation Introduction

(a)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(b)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(c)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(d)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

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Answer 4

Question

Chapter C, Problem C.20P

Interpretation Introduction

(a)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(b)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(c)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(d)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

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Answer 5

Chapter C, Problem C.20P

Interpretation Introduction

(a)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(b)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(c)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Interpretation Introduction

(d)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Answer 6

Chapter C, Problem C.20P

Interpretation Introduction

(a)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Answer 7

Chapter C, Problem C.20P

Interpretation Introduction

(a)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Answer 8

Interpretation Introduction

(b)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Answer 9

Interpretation Introduction

(b)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Answer 10

Interpretation Introduction

(c)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Answer 11

Interpretation Introduction

(c)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Answer 12

Interpretation Introduction

(d)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Answer 13

Interpretation Introduction

(d)

Interpretation:

Each asymmetric carbon in the given molecule is to be assigned R or S configuration.

Concept introduction:

The four groups attached to an asymmetric carbon are assigned priorities on the basis of the atomic number of the atom that is directly attached. In the case of a tie, the atoms one bond away are compared. If the priority groups 1 to 3 are arranged clockwise with the lowest priority group at the back, the asymmetric carbon is assigned an R configuration. If they are arranged counterclockwise, the configuration is S.

When writing the IUPAC name of a molecule, each R and S designation can be written immediately before the first number used to locate the substituent attached to the asymmetric carbon atom. An alternate way is to write all the R and S designations together at the front of the name. The locator number for each asymmetric carbon atom must appear before its R or S designation and the designations must be separated from each other by a comma.

Answer 14

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Answer 15

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Answer 16

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Answer 17

Ch. C - Prob. C.1P Ch. C - Prob. C.2P Ch. C - Prob. C.3P Ch. C - Prob. C.4P Ch. C - Prob. C.5P Ch. C - Prob. C.6P Ch. C - Prob. C.7P Ch. C - Prob. C.8P Ch. C - Prob. C.9P Ch. C - Prob. C.10P

Solution Summary: The author explains that each asymmetric carbon in the given molecule is assigned R or S configuration. Priorities are assigned on the basis of atomic numbers of the atoms directly attached.

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