ORGANIC CHEMISTRY
ORGANIC CHEMISTRY
6th Edition
ISBN: 9781266633973
Author: SMITH
Publisher: MCG
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Chapter 1, Problem 40P

Citric acid is responsible for the tartness of citrus fruits, especially lemons and limes.

Chapter 1, Problem 40P, Citric acid is responsible for the tartness of citrus fruits, especially lemons and limes. a.What is

a. What is the molecular formula of citric acid?

b. How many lone pairs are present?

c. Draw a skeletal structure.

d. How many s p 2 hybridized carbon atoms are present?

e. What orbitals are used to form each indicated bond ( [ 1 ] [ 4 ] ) ?

Expert Solution
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Interpretation Introduction

(a)

Interpretation: The molecular formula of citric acid is to be stated.

Concept introduction: In ball-and-stick model, each colored ball represents a specific atom and each stick represents a bond. In this model, each black ball represents C atoms, each gray ball represents H atoms, and each red ball represents O atoms.

Answer to Problem 40P

The molecular formula of citric acid is C6H8O7.

Explanation of Solution

The given ball-and-stick model of citric acid is,

ORGANIC CHEMISTRY, Chapter 1, Problem 40P , additional homework tip  1

Figure 1

In ball-and-stick model, each colored ball represents a specific atom and each stick represents a bond. In this model, each black ball represents C atoms, each gray ball represents H atoms, and each red ball represents O atoms.

In the above model,

• There are seven red balls. Thus, there are seven O atoms.

• There are six black balls. Thus, there are six C atoms.

• There are eight grey balls. Thus, there are eight H atoms.

Hence, the molecular formula of citric acid is C6H8O7.

Conclusion

The molecular formula of citric acid is C6H8O7.

Expert Solution
Check Mark
Interpretation Introduction

(b)

Interpretation: The number of lone pairs present in citric acid is to be stated.

Concept introduction: In a compound or molecule, the lone pairs represent number of unshared electrons on atom. An atom may or may not have unshared electrons. For example, carbon and hydrogen atoms have no lone pair but each oxygen atom has two lone pairs.

Answer to Problem 40P

There are total 14 lone pairs in citric acid.

Explanation of Solution

The molecular formula of citric acid is C6H8O7. Carbon and hydrogen atoms have no lone pair, but each oxygen atom has two lone pairs. There are seven oxygen atoms in citric acid. Thus, there are total 14 lone pairs (7×2=14) in citric acid.

Conclusion

There are total 14 lone pairs in citric acid.

Expert Solution
Check Mark
Interpretation Introduction

(c)

Interpretation: A skeletal structure of citric acid is to be drawn.

Concept introduction: A ball-and-stick model is converted into skeletal structure by replacing black ball with C, gray ball with H, and red ball with O. Omit the H atom on carbon, but not in the case of heteroatom.

Answer to Problem 40P

A skeletal structure of citric acid is,

ORGANIC CHEMISTRY, Chapter 1, Problem 40P , additional homework tip  2

Explanation of Solution

In ball-and-stick model each colored ball represents a specific atom and each stick represents a bond. A ball-and-stick model is converted into skeletal structure by replacing black ball with C, gray ball with H, red ball with O, and blue ball with N. Omit the H atom on carbon, but not in the case of heteroatom.

A skeletal structure of citric acid is shown in Figure 2.

ORGANIC CHEMISTRY, Chapter 1, Problem 40P , additional homework tip  3

Figure 2

Conclusion

In ball-and-stick model each colored ball represents a specific atom and each stick represents a bond.

Expert Solution
Check Mark
Interpretation Introduction

(d)

Interpretation: The number of sp2 hybridized carbon in citric acid is to be stated.

Concept introduction: According to the rule of hybridization, an atom that is surrounded with two groups is sp hybridized, an atom that is surrounded with three groups is sp2 hybridized, and an atom that is surrounded with four groups is sp3 hybridized.

Answer to Problem 40P

There are three sp2 hybridized carbon atoms in citric acid.

ORGANIC CHEMISTRY, Chapter 1, Problem 40P , additional homework tip  4

Explanation of Solution

The Lewis structure of citric acid is,

ORGANIC CHEMISTRY, Chapter 1, Problem 40P , additional homework tip  5

Figure 3

According to the rules of hybridization, an atom that is surrounded with two groups is sp hybridized, an atom that is surrounded with three groups is sp2 hybridized, and an atom that is surrounded with four groups is sp3 hybridized.

The sp2 hybridized carbon atoms (surrounded by three groups) are shown in Figure 4.

ORGANIC CHEMISTRY, Chapter 1, Problem 40P , additional homework tip  6

Figure 4

Thus, there are three sp2 hybridized carbon atoms in citric acid.

Conclusion

There are three sp2 hybridized carbon atoms in citric acid.

Expert Solution
Check Mark
Interpretation Introduction

(e)

Interpretation: The orbitals that are used to form each indicated bond is to be stated.

Concept introduction: According to the rule of hybridization, an atom that is surrounded with two groups is sp hybridized, an atom that is surrounded with three groups is sp2 hybridized, and an atom that is surrounded with four groups is sp3 hybridized.

Answer to Problem 40P

Bond [1] is formed by Csp2Osp2 hybridized orbitals. Bond [2] is formed by Csp2Csp3 hybridized orbitals. Bond [3] is formed by Osp3H1s orbitals. Bond [4] is formed by Csp3Osp3 hybridized orbitals.

Explanation of Solution

Bond [1] represents C=O bond, in which both carbon atom and oxygen atom are sp2 hybridized. Thus, it is formed by Csp2Osp2 hybridized orbitals.

Bond [2] represents bonding between the carbon atom of carbonyl group (C=O), and the carbon atom of CH2 group. The carbon atom of carbonyl group is sp2 hybridized and the carbon atom of CH2 group is sp3 hybridized.

Thus, [2] is formed by Csp2Csp3 hybridized orbitals.

Bond [3] represents, OH bond. This bond is formed through sp3 hybridized orbital of oxygen and 1s orbital of hydrogen.

Thus, [3] is formed by Osp3H1s orbitals.

Bond [4] represents, CO bond, in which both carbon atom and oxygen atom are sp3 hybridized. Thus, [4] is formed by Csp3Osp3 hybridized orbitals.

Conclusion

The number of surrounded group around any atom predicts the hybridization of that atom, which is further helpful to predict the orbitals involve in bond formation.

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a) Consider a molecule of acetone cyanohydrin, shown below. What is the hybridization and molecular geometry at CA, CB, and O?  (b) For Carbon B (CB) and nitrogen (N), draw orbital energy diagrams showing the orbitals involved in bonding after hybridization. Be sure to fill the orbitals appropriately with valence electrons. c) In your diagrams in part (b), which orbitals are involved in sigma and pi bonding?            Orbitals Involved in Sigma Bonding                                       Orbitals Involved in Pi Bonding  2p sp sp2 sp3 2p sp sp2 sp3 (d) In a sample containing many molecules of acetone cyanohydrin (and no other substances), what type(s) of intermolecular forces could be present? Choose all that apply. Covalent Bonds            Hydrogen Bonds              Dipole-Dipole Forces              London Dispersion Forces
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1. Calculate the percentage s and p characters in sp, sp^2 and sp^3 hybrid orbitals. 2. Draw the molecular orbital diagram of propene, CH3-CH=CH2. 3. Draw an orbital diagram of an allene, H2C=C=CH2. What hybridization must the central carbon atom have in order to form two double bonds? 4. Describe the shape of sp^3 hybrid orbitals. 5. Dicuss, with illustrations, the two main steps in the hybridization of a carbon atom. 6.a. Arrange the following organic molecules in order of increasing acidity, starting with the least acidic. CH3CH3, HC(=_)CH and CH2=CH2 b. How many hybrid orbitals are formed when one 2s atomic orbital mixes with two 2p atomic orbitals? What shape do they form? c. Describe in detail, the shape of p atomic orbitals. d. Giving an example, explain what is meant by the excited-state electronic configuration of an atom of an element. e. Using clear illustrations, discuss the main differences between E1 and E2 mechanisms in organic reactions.

Chapter 1 Solutions

ORGANIC CHEMISTRY

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