![Organic Chemistry](https://www.bartleby.com/isbn_cover_images/9781118133576/9781118133576_largeCoverImage.gif)
Concept explainers
Interpretation:
The synthesis of the given compound from benzene is to be suggested.
Concept introduction:
Electrophiles are electron-deficient species that has positive or partially positive charge. Lewis acids are electrophiles that accept electron pair.
Nucleophiles are electron-rich species that has negative or partially negative charge. Lewis bases are nucleophiles that donate electron pair.
Free radical is an atom, molecule, or ion that has unpaired electrons, which makes it highly chemically reactive.
Substitution reaction: A reaction in which one of the hydrogen atoms of a hydrocarbon or a
Elimination reaction: A reaction in which two substituent groups are detached and a double bond is formed is called elimination reaction.
Addition reaction: It is the reaction in which unsaturated bonds are converted to saturated molecules by the addition of molecules.
The electrophilic
Electrophilic substitution reaction is the type of reaction in which an electrophile displaces hydrogen from the compound.
Nucleophilic aromatic substitution reaction is based on the addition-elimination mechanism.
Activating groups give substitution at the ortho and para positions.
Chlorine is the activating group. It gives two products; one ortho substituted, and the other para substituted.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 21 Solutions
Organic Chemistry
- Following is the structural formula of the tranquilizer meparfynol (Oblivon). Propose a synthesis for this compound starting with acetylene and a ketone. (Notice the -yn- and -ol in the chemical name of this compound, indicating that it contains alkyne and hydroxyl functional groups.)arrow_forwardProvide the reagents for the reactions.arrow_forwardWhat reactions and reagents can be used to make phenol from benzene if electrophilic aromatic substitution reactions are excluded and benzene is the only source of carbon?arrow_forward
- When 2-chloropropane treated with NaOH and 1-chloropropane treated with NaOH separately produce two different functional groups. Provide both reactions and explain the two different functional groups produced.arrow_forwardSynthesize each compound.You may use benzene, acetylene (HC≡CH), ethanol, ethylene oxide, and any inorganic reagents.arrow_forwardSuggest a method of preparing ethyl benzene, starting with benzene and ethylene as the only organic reagents.arrow_forward
- Following is the structural formula of the tranquilizer meparfynol (Oblivon). Oblivon HO Propose a synthesis for this compound starting with acetylene and a ketone. (Notice the -yn- and -ol in the chemical name of this compound, indicating that it contains al- kyne and hydroxyl functional groups.)arrow_forwardDiazomethane, CH2N2, is used in the organic chemistry laboratory despite its danger because it produces very high yields and is selective for reaction with carboxylic acids. Write the products of the following reactions.arrow_forwardWhen bromine is added to two beakers, one containing phenyl isopropyl ether and the other containing cyclohexene, the bromine color in both beakers disappears. What observation could you make while performing this test that would allow you to distinguish the alkene from the aryl ether?arrow_forward
- Outline syntheses of the following compounds, starting with triphenylphosphine, an alkyl halide and an aldehyde or ketone.a) 2-pentene b) Trans 1,2-diphenylethene c) Cyclohexylethenearrow_forwardElectrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the a position. Predict the major products of the reactions of naphthalene with fuming sulfuric acid.arrow_forwardProvide the product(s) for the reaction of benzene with nitric acid and sulfuric acid. If more than one product is formed, list the major product first. If no reaction, draw the starting material.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningMacroscale and Microscale Organic ExperimentsChemistryISBN:9781305577190Author:Kenneth L. Williamson, Katherine M. MastersPublisher:Brooks Cole
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305580350/9781305580350_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305577190/9781305577190_smallCoverImage.gif)