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Chapter 22: Problem 32

Draw structures for these alkyl and aryl halides. \begin{equation} \begin{array}{l}{\text { a. chlorobenzene }} \\ {\text { b. } 1 \text { -bromo-4-chlorohexane }} \\ {\text { c. } 1,2 \text { -difluoro-3-iodocyclohexane }} \\ {\text { d. } 1,3 \text { -dibromobenzene }} \\ {\text { e. } 1,1,2,2 \text { - tetrafluoroethane }}\end{array} \end{equation}

Short Answer

Expert verified
The structures are: a. chlorobenzene, b. 1-bromo-4-chlorohexane, c. 1,2-difluoro-3-iodocyclohexane, d. 1,3-dibromobenzene, e. 1,1,2,2-tetrafluoroethane.

Step by step solution

01

Drawing Chlorobenzene

Chlorobenzene is an aromatic compound where a chlorine atom replaces one hydrogen of the benzene ring. To draw chlorobenzene, begin with a hexagonal benzene ring structure (a six-carbon ring with alternating double bonds) and then substitute one hydrogen (usually at the first or any position) with a chlorine atom, denoted as 'Cl'.
02

Structuring 1-Bromo-4-chlorohexane

For 1-bromo-4-chlorohexane, start by drawing a six-carbon chain representing hexane. Number the carbon atoms from 1 to 6. Attach a bromine ('Br') atom to the first carbon and a chlorine ('Cl') atom to the fourth carbon. This results in halogenation at specified positions on the hexane.
03

Creating 1,2-Difluoro-3-iodocyclohexane

Identify cyclohexane as a six-carbon ring. Position the carbons in a sequential cyclic order and then attach fluorine ('F') atoms to the 1st and 2nd carbons, and an iodine ('I') atom to the 3rd carbon. This structure has specific halogen substitutions at defined positions on the cyclohexane ring.
04

Forming 1,3-Dibromobenzene

Draw the benzene ring first, which is a hexagon with alternating double bonds. Position two bromine ('Br') atoms on the benzene ring. Place them at the 1st and 3rd positions (meta position). There is one bromine on each carbon, three carbons apart.
05

Sketching 1,1,2,2-Tetrafluoroethane

Begin with a two-carbon chain representing ethane. On the first carbon, attach two fluorine ('F') atoms, and on the second carbon, attach another two fluoro atoms. This results in two carbons each bearing two fluorine atoms, making tetrafluorination on the ethane molecule.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Alkyl Halides
Alkyl halides are organic compounds that contain at least one halogen atom bonded to an alkyl group. An alkyl group is essentially an alkane minus one hydrogen atom. Halogens typically include chlorine, bromine, iodine, and fluorine. These compounds are named by replacing the -ane suffix of the parent alkane with the corresponding prefix for the halogen, such as fluoro-, chloro-, bromo-, or iodo-.
  • For example, in 1-bromo-4-chlorohexane, "hexane" refers to a six-carbon alkane chain.
  • The numbers indicate the positions of the bromine (at carbon 1) and the chlorine (at carbon 4) atoms on the alkane chain.
  • Alkyl halides can undergo various reactions, such as nucleophilic substitution and elimination reactions, which are fundamental in organic synthesis.
Alkyl halides are versatile starting materials that can be converted into many other types of organic compounds.
Aryl Halides
Unlike alkyl halides, aryl halides involve a halogen atom attached directly to an aromatic ring. In these compounds, the halogen is bonded to a carbon that is part of the aromatic system, usually a benzene ring. Because of the stability of the aromatic structure, aryl halides can display unique reactivity compared to alkyl halides.
  • An example is chlorobenzene, where the benzene ring is substituted with a chlorine atom.
  • Due to the resonance stability of aromatic rings, aryl halides are less reactive in comparison to alkyl halides when it comes to nucleophilic substitution reactions.
  • They play a significant role in the synthesis of dyes, pharmaceuticals, and other complex molecules.
Aryl halides are a cornerstone in industrial applications, often serving as intermediates in various chemical processes.
Chemical Structure Drawing
Drawing chemical structures is an essential skill in organic chemistry that helps visualize molecular geometry and functional groups. Accurate chemical drawings are crucial for understanding the reactivity and properties of compounds.
  • Start by identifying the main framework of the molecule, such as a benzene ring or carbon chain.
  • Next, add any substituents like halogens in the correct positions from the functional group name, e.g., placing Br and Cl on the designated carbons in 1-bromo-4-chlorohexane.
  • Consider the orientations and angles, ensuring to depict rings as cyclic structures.
This skill is invaluable for predicting reaction products and planning synthetic routes.
Halogenation
Halogenation is a chemical reaction that introduces one or more halogen atoms into a compound. In halogenation, alkanes or alkenes are usually reacted with halogen molecules like Cl_2 or Br_2.
  • The process involves the replacement of a hydrogen atom with a halogen atom.
  • Halogenation can occur under light or heat, especially when involving alkanes.
  • It provides a pathway to create a wide array of halogenated compounds, such as in creating 1,1,2,2-tetrafluoroethane, where fluorine replaces hydrogen atoms on the ethane molecule.
This transformation is pivotal for making materials used in refrigerants, polymers, and many other industrial chemicals.
Aromatic Compounds
Aromatic compounds are characterized by their stable ring structures with alternating double bonds, known as aromaticity. Benzene is the simplest example, and its derivatives form the basis for many essential chemicals.
  • Common features include a hexagonal ring structure with delocalized electrons, which contributes to their unique stability and reactivity.
  • The nature of the pi-bond cloud means that electrophilic substitution reactions are favored, a typical reaction path for modifying these compounds.
  • Aromaticity is a criterion where a compound contains a cyclic, planar ring with a continuous pi-electron cloud, fulfilling H眉ckel's rule.
Such properties make aromatic compounds crucial in the production of polycyclic aromatic hydrocarbons, pharmaceuticals, and synthetic materials.

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Most popular questions from this chapter

Explain why the boiling points of alkyl halides increase in order going down the column of halides in the periodic table, from fluorine through iodine.

Infer why water-soluble organic compounds with carboxyl groups exhibit acidic properties in solutions, whereas similar compounds with aldehyde structures do not exhibit these properties.

Why do the following characteristics apply to transition metals? (Chapter 6\()\) \begin{equation} \begin{array}{l}{\text { a. Ions vary in charge. }} \\ {\text { b. Many of their solids are colored. }} \\ {\text { c. Many are hard solids. }}\end{array} \end{equation}

Draw structures for each of the following carbonyl compounds. \begin{equation} \begin{array}{l}{\text { a. } 2,2 \text { -dichloro-3 -pentanone }} \\ {\text { b. } 4 \text { -methylpentanal }} \\ {\text { c. isopropyl hexanoate }} \\\ {\text { d. octanoamide }} \\ {\text { e. } 3 \text { -fluoro- } 2 \text { -methylbutanoic acid }} \\ {\text { g. cyclopentanal }} \\ {\text { f. hexyl methanoate }}\end{array} \end{equation}

Describe the properties of carboxylic acids.
See all solutions

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