Question

Is the enthalpy of the Diels-Alder reaction positive or negative? Is the entropy of the Diels-Alder...

Is the enthalpy of the Diels-Alder reaction positive or negative? Is the entropy of the Diels-Alder reaction positive or negative? In each case, clearly explain why it is positive or negative.

Homework Answers

Answer #1

a) Entropy: negative

In this reaction, the degree of freedom decreases as the reactants are converted into the products. The reactions therefore, represents an example of decrease in entropy, S is negative.

no of product moles < no of reactant moles

b) Enthalpy : positive

in order to diels alder reaction occur we need to supply heat of light . diels alder reaction some are thermally allowed and some are photochemically allowed. in both cases heat must be supplied so it is Endothermic

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Diels Alders Reaction While performing the Diels-Alder reaction between cyclopentadiene and maleic anhydride: (a) Why do...
Diels Alders Reaction While performing the Diels-Alder reaction between cyclopentadiene and maleic anhydride: (a) Why do you have to crack the diene? Draw the reaction that occurs during the cracking process   
(1) Draw the products of Diels-Alder reaction of maleic anhydride with α-phellandrene, β- phellandrene, and α-terpinene,...
(1) Draw the products of Diels-Alder reaction of maleic anhydride with α-phellandrene, β- phellandrene, and α-terpinene, assuming that endo product is formed. In each structure, mark all chiral carbons present (if any). (2) Using a reaction of 1,3-cyclohexadiene with maleic anhydride, explain endo selectivity in Diels-Alder reaction (include a clear drawing of orbitals overlap in transition state as a part of your answer)
In a Diels Alder Reaction, if you had a mixture of the anhydride and the diacid...
In a Diels Alder Reaction, if you had a mixture of the anhydride and the diacid and you were going to use either aqueous acid or aqueous base to separate the 2 compounds, which aqueous solution would you use and why?
In a Diels-Alder reaction with benzyne and anthracene to make triptycene, why is the benzyne added...
In a Diels-Alder reaction with benzyne and anthracene to make triptycene, why is the benzyne added to the central ring of anthracene and not on the ends? Which resonance structure of anthracene is the most stable?
Explain in terms of thermodynamic parameters, how it is possible for a Diels-Alder reaction to proceed...
Explain in terms of thermodynamic parameters, how it is possible for a Diels-Alder reaction to proceed in the forward direction (cycloaddition) at room temperature, but in the reverse direction (decomposition of the adduct) at higher temperatures
how does hydrophobic effect result in a rate acceleration of Diels-Alder reaction?
how does hydrophobic effect result in a rate acceleration of Diels-Alder reaction?
the detail mecanism of furan and maleimide diels alder reaction to form endo and exo adduct
the detail mecanism of furan and maleimide diels alder reaction to form endo and exo adduct
How can you tell if Diels- Alder reaction has gone all the way to completion or...
How can you tell if Diels- Alder reaction has gone all the way to completion or not?
Diels Alder Reaction with anthracene and maleic anhydride Show the result of the hydrolysis of the...
Diels Alder Reaction with anthracene and maleic anhydride Show the result of the hydrolysis of the reactin product. Why aren't we worried about exposing the product of the reaction to atmospheric moisture during this experiment, since water will destroy the desired product? How would you distinguish whether this degradation of the product had occurred using instruments available in organic chemistry lab?
Furan and maleimide undergo a Diels–Alder reaction at 25 °C to give the endo isomer of...
Furan and maleimide undergo a Diels–Alder reaction at 25 °C to give the endo isomer of the product. When the reaction takes place at 70 °C, however, the major product is the exo isomer. Further study shows that the endo isomer of the product isomerizes to the exo isomer at 70 °C. a)Using free energy diagram(s) explain why the endo isomer predominates when the reaction takes place at 25 °C and why the exo isomer predominates at 70 °C. Explain...
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT