Answer: Benzene is less reactive than methylbenzoate and more reactive than Nitrobenzene
Explanation:
This is because the methyl group on the benzene ring is an electron donating group leading to the activation of the ring and subsequently leading to more canonical resonance structure at the intermediate stage of the reaction enhancing the faster reactivity
However for the Nitrobenzene the nitro group is an electron withdrawing group leading to a slower activation and less resonance canonical structure at the reaction intermediate leading to a slower reaction than the reaction of benzene without the nitro group
<span>The particles are far apart from each other.</span>
Answer: All of these statements are true
Explanation:
Melting point help us to determine if a mixture is pure or has impurities by the virtues of it melting range..
Energy required=mass*specific heat*temperature change
=10*4.184*57.2
=2393.248j
=2.39*10^3
Answer:the pH is 12
Explanation:
First We need to understand the structure of trimethylamine
Due to the grades of the bond in the nitrogen with a hybridization sp3 is 108° approximately, then is generated a dipole magnetic at the upper side of the nitrogen, this dipole magnetic going to attract a hydrogen molecule of the water making the water more alkaline
C3H9N+ H2O --> C3H9NH + OH-
![k=\frac{[C3H9NH]*[OH-]}{[C3H9N]}](https://tex.z-dn.net/?f=k%3D%5Cfrac%7B%5BC3H9NH%5D%2A%5BOH-%5D%7D%7B%5BC3H9N%5D%7D)
Then:
The concentration of the trimethylamine is 0.3 and the concentration of the ion C3H9NH is equal to the OH- relying on the stoichiometric equation. We could find the concentration of the OH- ion with the square root of the multiplication between k and the concentration of trimethylamine
[OH-]=
[OH-]=0.01
pH=14-(-log[OH-])
pH=12