Related Experiment Video
Updated: Mar 8, 2026

Ammonia Synthesis at Low Pressure
Published on: August 23, 2017
Why Are Addition Reactions to N2 Thermodynamically Unfavorable?
1Department of Chemistry and the Center for Advanced Scientific Computing and Modeling, University of North Texas , 1155 Union Circle, #305070, Denton, Texas 76203-5070, United States.
Abstract:
Thermochemical data are used to show that, of the 89.9 kcal/mol difference between the endothermicity of H2 addition to N2 (ΔH = 47.9 kcal/mol) and the exothermicity of H2 addition to acetylene (ΔH = -42.0 kcal/mol), less than half is due to a stronger π bond in N2 than in acetylene. The other major contributor to the difference of 89.9 kcal/mol between the enthalpies of hydrogenation of N2 and acetylene is that the pair of N-H bonds that are created in the addition of H2 to N2 are significantly weaker than the pair of C-H bonds that are created in the addition of H2 to acetylene. The reasons for this large difference between the strengths of the N-H bonds in E-HN═NH and the C-H bonds in H2C═CH2 are analyzed and discussed.
Related Concept Videos
Free Energy Changes for Nonstandard States
Radical Anti-Markovnikov Addition to Alkenes: Thermodynamics
Introduction to Electrophilic Addition Reactions of Alkenes
Addition and elimination...
Acids, Bases and Neutralization Reactions
Acids, Bases and Neutralization Reactions
Rate-Determining Steps
In a multistep reaction mechanism, one of the elementary steps progresses significantly slower than the others. This slowest step is called the rate-limiting step (or rate-determining step). A reaction cannot proceed faster than its slowest step, and hence, the rate-determining step limits the overall reaction rate.
The concept of rate-determining step can be understood from the analogy of a 4-lane freeway with a short-stretch of traffic-bottleneck caused due to...

