Answer:
Here's what I get
Explanation:
1. Balanced equation
HQ⁻ + CH₃-Br ⟶ HQ-CH₃ + Br⁻
(I must use HQ because the Brainly Editor thinks the O makes a forbidden word)
2. Mechanism
HQ⁻ + CH₃-Br ⟶[HQ···CH₃···Br]⁻⟶ HQ-CH₃ + Br⁻
A C B
The hydroxide ion attacks the back side of the carbon atom in the bromomethane (A).
At the same time as the Q-H bond starts to form, the C-Br bond starts to break.
At the half-way point, we have a high-energy intermediate (C) with partially formed C-O and C-Br bonds.
As the reaction proceeds further, the Br atom drops off to form the products — methanol and bromide ion (B).
3. Energy diagram
See the diagram below.
Centimeters are units of length.
I will assume that the sign ? between the C and the CCH3 is a triple bond, and I will represent it by three vertical lines |||
So the reaction is:
<span>CH3CH2CH2CH2C ||| CCH3+2Br2 ---->
This is a typical reaction known as halogenation of alkines.
This is an addition reaction, i.e. the alkyne undergoes an addition of the Br2 (and it also happens with Cl2) to the triple bond to form a tetra halide.
.
Br Br
</span> | |
<span><span>CH3CH2CH2CH2C ||| CCH3+2Br2 ----> CH3 CH2 CH2 CH2 C - C</span> - CH3
| |
Br Br
</span>
Answer:
it's law
Explanation:
i got it wrong because i put the wrong answer but it was law or c
i hope this help's
