Textbook Question
How does the carbonyl in mCPBA weaken the O―O σ bond (i.e., make a better leaving group)?
1
views
Ch. 9 - Alkenes II: Oxidation and Reduction
Mullins1st EditionOrganic Chemistry: A Learner Centered ApproachISBN: 9780137566471
Not the one you use?Change textbookSelect a different textbook
Table of contents
- Ch. 2 - General Chemistry Translated: Finding the Electrons114
- Ch. 3 - Alkanes and Cycloalkanes: Properties and Conformational Analysis109
- Ch. 4 - Acids and Bases: Electron Flow144
- Ch. 5 - Chemical Reaction Analysis: Thermodynamics and Kinetics118
- Ch. 6 - Stereoisomerism: Arrangement of Atoms in Space112
- Ch. 7 - Principles of Green (Organic) Chemistry3
- Ch. 8 - Alkenes I: Properties and Electrophilic Additions158
- Ch. 9 - Alkenes II: Oxidation and Reduction150
- Ch. 10 - Alkynes: Electrophilic Addition and Redox Reactions101
- Ch. 11 - Properties and Synthesis of Alkyl Halides: Radical Reactions108
- Ch. 12 - Substitution and Elimination: Reactions of Haloalkanes172
- Ch. 13 - Alcohols, Ethers and Related Compounds: Substitution and Elimination239
- Ch. 14 - Structural Identification I: Infrared Spectroscopy and Mass Spectrometry54
- Ch. 15 - Structural Identification II: Nuclear Magnetic Resonance Spectroscopy93
- Ch. 16 - Metals in Organic Chemistry48
- Ch. 17 - Carbonyl Addition Reactions: Aldehydes and Ketones45
- Ch. 18 - Nucleophilic Acyl Substitution I: Carboxylic Acids18
- Ch. 19 - Nucleophilic Acyl Substitution II: Carboxylic Acid Derivatives39
- Ch. 20 - Enolates: Carbonyl Addition and Substitution13
- Ch. 21 - Conjugated Systems I: Stability and Addition Reactions56
- Ch. 22 - Conjugated Systems II: Pericyclic Reactions54
- Ch. 23 - Benzene I: Aromatic Stability and Substitution Reactions64
- Ch. 24 - Benzene II: Reactions Influenced by the Aromatic Ring62
- Ch. 25 - Amines: Structure, Reactions, and Synthesis27
- Ch. 26 - Amino Acids, Proteins, and Peptide Synthesis9
- Ch. 27 - Carbohydrates, Nucleic Acids, and Lipids54
Mullins1st EditionOrganic Chemistry: A Learner Centered ApproachISBN: 9780137566471Not the one you use?Change textbook
Chapter 8, Problem 13a
Suggest an alkene that could be used to make each of the following halohydrins.
(a) 
Verified step by step guidance1
Identify the structure of the halohydrin provided in the problem. A halohydrin is an organic compound containing both a hydroxyl group (-OH) and a halogen atom (e.g., Cl, Br) on adjacent carbon atoms.
Determine the position of the hydroxyl group (-OH) and the halogen atom in the halohydrin. This will help you identify the carbon-carbon double bond (alkene) that could lead to this product.
Recall that halohydrins are typically formed through the reaction of an alkene with a halogen (e.g., Br2 or Cl2) in the presence of water. The reaction follows a regioselective and anti-addition mechanism.
Work backward to deduce the structure of the alkene. Remove the -OH group and the halogen atom from the halohydrin, and replace them with a double bond between the two adjacent carbon atoms.
Verify the structure of the proposed alkene by considering the regioselectivity and stereochemistry of the halohydrin formation reaction. Ensure that the alkene you suggest would lead to the given halohydrin under the reaction conditions.
Verified video answer for a similar problem:
This video solution was recommended by our tutors as helpful for the problem above.
Video duration:
4mWas this helpful?
Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Alkenes
Alkenes are hydrocarbons that contain at least one carbon-carbon double bond (C=C). They are unsaturated compounds, meaning they have fewer hydrogen atoms than alkanes. The presence of the double bond makes alkenes reactive, allowing them to undergo various addition reactions, which are crucial for synthesizing other organic compounds, including halohydrins.
Recommended video:
2:09
Alkene Metathesis Concept 1
Halohydrin Formation
Halohydrins are compounds formed when alkenes react with halogens and water. This reaction typically involves the electrophilic addition of a halogen (like Br or Cl) followed by the nucleophilic attack of water, resulting in the formation of a halohydrin. Understanding the mechanism of this reaction is essential for predicting which alkene can yield a specific halohydrin.
Recommended video:
Guided course
01:44General properties of halohydrin formation.
Regioselectivity
Regioselectivity refers to the preference of a chemical reaction to yield one structural isomer over others when multiple products are possible. In the context of halohydrin formation, the regioselectivity is influenced by the stability of the carbocation intermediate formed during the reaction. Recognizing how different alkenes can lead to different regioisomers is key to selecting the appropriate alkene for a desired halohydrin.
Recommended video:
Guided course
05:09Heck Reaction
Related Practice
Textbook Question
Suggest an alkene that could be used to make each of the following halohydrins.
(c)
1
views
Textbook Question
Predict the product(s) of each of the following reactions, making sure to indicate the relative stereochemical outcome. Indicate any racemic mixtures by drawing both enantiomers.
(a)
4
views
Textbook Question
Calculate the atom economy of the reaction in Figure 9.24. [Catalysts are not included in the atom economy calculation.]
2
views
Textbook Question
Provide arrow-pushing mechanisms for Assessments 9.10(b) and 9.10(c) that rationalize the regioselective and stereospecific formation of each halohydrin.
(b)
(c)
2
views
Textbook Question
Explain why water attacks the carbon of the bromonium ion as opposed to the bromonium ion itself in the second step of halohydrin formation.
2
views