Answer: A. The reaction takes place in one step.
Explanation:
Rate law says that rate of a reaction is directly proportional to the concentration of the reactants each raised to a stoichiometric coefficient determined experimentally called as order.
Molecularity of the reaction is defined as the number of atoms, ions or molecules that must colloid with one another simultaneously so as to result into a chemical reaction.
Order of the reaction is defined as the sum of the concentration of terms on which the rate of the reaction actually depends. It is the sum of the exponents of the molar concentration in the rate law expression.
Elementary reactions are defined as the reactions for which the order of the reaction is same as its molecularity and order with respect to each reactant is equal to its stoichiometric coefficient as represented in the balanced chemical reaction.
![Rate=k[A]^a[B]^b](https://tex.z-dn.net/?f=Rate%3Dk%5BA%5D%5Ea%5BB%5D%5Eb)
k= rate constant
a= order with respect to A
b = order with respect to B
Answer:
a) After the balloon inflated after 440 uL of dropwise due to the reaction of 1-Decene and the solution in the conical vial. b) 
⇒ 16
c) No 
was not the limiting reactant.
Explanation:
Generally, hydrogenation is the chemical reaction between a compound or element and molecular hydrogen in the presence of catalysts such as platinum.
a) After the balloon inflated after 440 uL of dropwise 1-Decene solution was added due to the reaction between 1-Decene and the solution in the conical vial.
b) ⇒ 16
c) was not the limiting reactant based on the mol to mol ratio of and decane which is 1:1. Therefore, if 0.8 mol of decane was produced then 0.8 mol of would also be produced.
Answer:
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Explanation:
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The question is incomplete. Complete question is attached below
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Correct Answer:
Option C i.e. I ~ III < IV < V < II
Reason:
During a nucleophilic subsitution reaction of chloroarenes, Cl- group is replaced by an nucleophile like OH-.
Order of reactivity, during such reactions depends on the electron density on carbon atom that is attached to Cl. Lower the electron density, greater will be the reactivity.Among the provided chloroarenes, electron density on C atom will be minimum in case of compound II, because of presence of electron withdrawing group (-NO2) at ortho and para position. Due to this, there will be large number of resonating structures. This signifies greater electron de-localization, and hence largest reactivity for nucleophilic substitution reaction.
Followed by this, compound V will show greater reactivity, due to presence of -NO2 group at para and one of the ortho position. Compound IV will have less number of resonating structures as compared to compound II and V, hence it will display poor reactivity towards nucleophilic substitution reaction.
Finally, compound 1 and III will minimum reactivity towards nucleophilic substitution reaction, because -NO2 group present at meta position (compound III) will not participate in resonance.
