Particles as small as atoms exist.
Answer:
1) The overlap of the p orbitals of the carbon-carbon π bond would be lost
Explanation:
Unlike simple bonds, a double bond can not rotate, since it is not possible to twist the ends of the molecule without breaking the π bond.
In the structure of but-2-ene present in the attachment, we can see the two isomers, <em>cis</em> and<em> trans</em>. These isomers cannot be interconverted by rotation around the carbon-carbon double bond without breaking the π bond.
Answer:
Ca(OH)₂ (aq) + 2NH₄Cl (aq) → CaCl₂ (aq) + 2NH₃ (g) + 2H₂O (l)
Ca²⁺ + 2OH⁻ + 2NH₄⁺ + 2Cl⁻ → Ca⁺² + 2Cl⁻ + 2NH₃ (g) + 2H₂O (l)
2OH⁻ + 2NH₄⁺ → 2NH₃ (g) + 2H₂O (l)
Is that high school stuff or college?
Answer:
The correct option is;
The reaction pathway for the trials is different
Explanation:
The effect of a catalyst in a chemical reaction is to increase the rate of a reaction by changing the pathway or mechanism of the reaction and/or to lower the transition state's energy thereby lowering the activation energy of the reaction
The pathway of the reaction is changed by the catalyst by the formation of intermediate compounds by the catalyst which require lower activation energy to form the products than the original non-catalyzed reactants. In the process the catalyst is regenerated, thereby, not taking part in the reaction.