catalyst The steric strain in the trisubstituted alkene makes the reaction exergonic. O The reaction is exergonic due to the reduction in angle strain in the product. O The alkene in the product has more stable bonding thane alkene in the starting material. O The use of the catalyst makes the reaction exergonic. O The product is more stable than the starting material making the reaction endergonic.

catalyst The steric strain in the trisubstituted alkene makes the reaction exergonic. O The reaction is exergonic due to the reduction in angle strain in the product. O The alkene in the product has more stable bonding thane alkene in the starting material. O The use of the catalyst makes the reaction exergonic. O The product is more stable than the starting material making the reaction endergonic.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter4: Organic Compounds: Cycloalkanes And Their Stereochemistry

Section4.3: Stability Of Cycloalkanes: Ring Strain

Problem 8P: Each Hâ†”H eclipsing interaction in ethane costs about 4.0 kJ/mol. How many such interactions are...

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