We are given the rate law, so we can substitute the given values for the rate constant and the concentrations of the reactants to solve for the rate of reaction. Since rate = k [NH4+][NO2-]:
rate = (2.7 x 10^-4 / M-s)(0.050 M)(0.25 M) = 3.375 x 10^-6 M/s
Constraints refers to demarcations of geometrical charecteristics between two or more entities or solid modeling bodies
Answer:
See the image 1
Explanation:
If you look carefully at the progress of the SN2 reaction, you will realize something very important about the outcome. The nucleophile, being an electron-rich species, must attack the electrophilic carbon from the back side relative to the location of the leaving group. Approach from the front side simply doesn't work: the leaving group - which is also an electron-rich group - blocks the way. (see image 2)
The result of this backside attack is that the stereochemical configuration at the central carbon inverts as the reaction proceeds. In a sense, the molecule is turned inside out. At the transition state, the electrophilic carbon and the three 'R' substituents all lie on the same plane. (see image 3)
What this means is that SN2 reactions whether enzyme catalyzed or not, are inherently stereoselective: when the substitution takes place at a stereocenter, we can confidently predict the stereochemical configuration of the product.
Answer:
Decomposition
Explanation:
H2CO3 Breaks down to H2O and CO2
Instinct to learning.
Please vote my answer branliest! Thanks.