Problem 62
Question
Wurtz reaction involves the reduction of alkyl halide with (a) HI (b) \(\mathrm{Zn} / \mathrm{HCl}\) (c) \(\mathrm{Zn}\) in an inert solvent (d) Na in ether
Step-by-Step Solution
Verified Answer
The Wurtz reaction involves Na in ether.
1Step 1: Understanding the Wurtz Reaction
The Wurtz reaction is a coupling reaction used in organic chemistry to form carbon-carbon bonds between alkyl halides using a metal.
2Step 2: Identifying the Correct Reactant
For the Wurtz reaction, sodium (Na) is typically used in an inert solvent like ether to couple two alkyl halides, forming a higher alkane.
3Step 3: Option Analysis
(a) HI is not used for coupling in Wurtz reaction. (b) Zn/HCl typically reduces carbonyl compounds and is not relevant to Wurtz. (c) Zn in inert solvent is not typically used for Wurtz reactions. (d) Na in ether is the correct option for carrying out the Wurtz reaction.
Key Concepts
Alkyl HalidesCarbon-Carbon BondsOrganic ChemistrySodium in EtherCoupling Reactions
Alkyl Halides
Alkyl halides are organic compounds where one or more halogen atoms are attached to an alkyl group. These halogens could be fluorine, chlorine, bromine, or iodine. They are pivotal in numerous chemical reactions due to their reactivity. In the Wurtz reaction, alkyl halides serve as starting materials.
- Alkyl group typically consists of carbon and hydrogen atoms.
- Halogens attached make these molecules amenable to substitutions and eliminations.
Carbon-Carbon Bonds
The formation of carbon-carbon bonds is central to organic chemistry as it leads to the creation of a vast array of complex molecules. These bonds are essential for building the backbone of organic structures.
- Strong and stable, they are the scaffolding of organic compounds.
- Key to synthesizing a wide variety of substances in pharmaceuticals, plastics, and more.
Organic Chemistry
Organic chemistry focuses on the study of carbon-based compounds. These range from simple molecules like methane to complex polymers and biochemical compounds.
- Deals primarily with carbon, hydrogen, and other elements such as oxygen, nitrogen, sulfur, and halogens.
- Involves understanding reactions such as substitutions, additions, and eliminations.
Sodium in Ether
In the context of the Wurtz reaction, sodium is used with an inert solvent like ether. This setup facilitates the coupling process. Ether serves as a solvent as well as a protective environment for the reaction.
- Natively, sodium is highly reactive, making ether a crucial component to moderate this reactivity.
- Ether stabilizes the reaction conditions, ensuring efficient formation of carbon-carbon bonds.
Coupling Reactions
Coupling reactions are essential tools in organic synthesis, used to join two molecules together with the formation of new chemical bonds. The Wurtz reaction is a classical coupling reaction, focusing on the creation of carbon-carbon bonds.
- Enables the construction of complex molecules from simpler units.
- Utilized in forming natural products, polymers, and various organic materials.
Other exercises in this chapter
Problem 60
Isopropyl chloride undergoes hydrolysis by (a) \(\mathrm{S}_{\mathrm{N}} \mathrm{t}\) and \(\mathrm{S}_{\mathrm{N}}\) mechanisms (b) neither \(\mathrm{S}_{\math
View solution Problem 61
Which one of the following is most reactive towards nucleophillic substitution reaction? (a) \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{Cl}\) (b) \(\mathrm{CH}_{2}
View solution Problem 63
Which of the following compound reacts with chlorobenzene to produce DDT? (a) trichloroacetaldehyde (b) m-chloroacetaldehyde (c) acetaldehyde (d) nitrobenzene
View solution Problem 64
Chloroform is slowly oxidized by air in the presence of light and air to form (a) phosgene (b) formyl chloride (c) formaldehyde (d) trichloroethanol
View solution