
(a)
Interpretation:
- The kinetic and
thermodynamic products of the given reaction has to be predicted.
Concept Introduction:
Reactions of conjugated dienes:
An electrophilic addition reaction to a conjugated diene forms both
Kinetic and thermodynamic products:
Kinetic product: The more rapidly formed product is called the kinetic product. The reactions that produce the kinetic product as the major product are said to be kinetically controlled. The kinetic product predominates when the reaction is irreversible.
Thermodynamic product: The more stable product is called the thermodynamic product. The reactions that produce the thermodynamic product as the major product are said to be thermodynamically controlled. The thermodynamic product predominates when the reaction is reversible. The thermodynamic product is the product with the most highly substituted double bond.
Rule: The stabilities of carbocation are,
(b)
Interpretation:
- The kinetic and thermodynamic products of the given reaction has to be predicted.
Concept Introduction:
Reactions of conjugated dienes:
An electrophilic addition reaction to a conjugated diene forms both
Kinetic and thermodynamic products:
Kinetic product: The more rapidly formed product is called the kinetic product. The reactions that produce the kinetic product as the major product are said to be kinetically controlled. The kinetic product predominates when the reaction is irreversible.
Thermodynamic product: The more stable product is called the thermodynamic product. The reactions that produce the thermodynamic product as the major product are said to be thermodynamically controlled. The thermodynamic product predominates when the reaction is reversible.
Rule: The stabilities of carbocation are,

Want to see the full answer?
Check out a sample textbook solution
Chapter 8 Solutions
ORGANIC CHEMISTRY-W/S.G+SOLN.MANUAL
- Problem 54, could you please explain it in detail? Thank you! Step by step, I'm really confused, so please don't make it overly complex. My question is to visually draw it out and demonstrate it to me; I'm confused about that problem, please (not just in words) but demonstrate it to me in all due essence (visually) with descriptions.arrow_forwardExplain the types of electromeric effects +E and -E.arrow_forwardBriefly describe the electromeric effect (Organic Chemistry)arrow_forward
- Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. (CH3)2NH, TSOH Drawingarrow_forwardSo, the first image is what I'm trying to understand regarding my approach. The second image illustrates my teacher's method, and the third image includes my notes on the concepts behind these types of problems.arrow_forwardHAND DRAWarrow_forward
- Draw a mental model for calcium chloride mixed with sodium phosphatearrow_forwardhere is my question (problem number 20) please explain to me thanks!arrow_forwardThe bromination of anisole is an extremely fast reaction. Complete the resonance structures of the intermediate arenium cation for the reaction (Part 1), and then answer the question that follows (Part 2).arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning

