From the reaction above, the rate is given by the following formula:
r = -(1/2) dA / dt = - dB / dt = (1/3) dC/ dt
Note that A and B charge is negative due to they decrease with time
given dA / dt = -0.110 M/s
hence dB / dt = -0.110 / 2 = -0.055 M/s
dC / dt = (-3/2) (-0.110) = 0.165 M/s
Answer:
The carbocation intermediate reacts with a nucleophile to form the addition product.
Explanation:
The reaction of benzene with an electrophile is an electrophillic substitution reaction. Here the electrophile replaces hydrogen. There is no formation of carbocation as intermediate in the reaction. Infact there is transition state where the electorphile attacks on benzene ring and at the same time the hydrogen gets removed from the benzene. So a transition carbocation is formed.
The general mechanism is shown in the figure.
i) Attack of the electrophile on the benzene (which is the nucleophile)
ii) The carbocation intermediate loses a proton from the carbon bonded to the electrophile.
iii) the carbocation formation is the rate determining step.
iv) There is no formation of addition product.
Thus the wrong statement is
The carbocation intermediate reacts with a nucleophile to form the addition product.
The balanced chemical equation for the production of chromium metal from the reaction of chromium(ll) nitrate reacts with a strip of zinc is:
3 Zn + 2 Cr(NO₃)₃ → 2 Cr + 3 Zn(NO₃)₂
This is a redox reaction, which <u>is a chemical reaction in which one or more electrons are transferred between the reagents</u>, causing a change in their oxidation states. In the proposed reaction, Cr oxidation state goes from +3 to 0, becoming metallic chromium, while Zn goes from being Zn⁰ to Zn²⁺.
<u>The mass of chromium metal produced in the above reaction will be,</u>
425.0 mL x x x x = 5.52 g
So, the mass of chromium metal produced when 425.0mL of 0.25M chromium(ll) nitrate reacts with a strip of zinc that remains in excess is 5.52 g of Cr.