Answer:
true
Explanation:
There are two electrons (in the 1s orbital) on both carbon and fluorine “shielding” the outer electrons from the full force of the nucleus and due to both atoms being approximately the same size (both period two) then it is this shielding effect and proton difference that is causing the electronegativity difference
City B is at a higher temperature because as you go higher in altitude the boiling point of water becomes lower.
This indicates that the reaction is exothermic meaning that it releases heat/energy
Answer:
The time taken for the cross to become invisible decreases.
Explanation:
We know that one of the factors affecting the rate of reaction is the concentration of reactants. From the collision theory, we know that the higher the concentration of reactants, the greater the possibility of effective collision between reactants leading ultimately to an increase in the rate of reaction. Increase in the rate of reaction implies that the reaction takes a shorter time to reach completion.
In the case of the reaction shown in the question, the point when the reaction is completed is observed by the time take for the cross mark to become invisible. If we look at the given data closely, we will notice that the volume of acid was held constant, the volume of thiosulphate was increased gradually while the volume of water was decreased accordingly. This implies that the concentration of the reactants was increased. Decreasing the volume of water increases reactant concentration.
As explained above, increase in reactant concentration increases the rate of reaction. Hence, the rate of reaction of the acid and thiosulphate increases as reactant concentration increases and the cross mark becomes invisible faster. This implies that in the last column for time taken for the cross to become invisible, the values of time decreases steadily as concentration of reactants increases.
Answer:
a) 2-bromopyrrole
Explanation:
Our options for this questions are:
a) 2-bromopyrrole
b) 2,3-dibromopyrrole
c) N-bromopyrrole
d) 3-bromopyrrole
To understand how the reaction works we have to start with the <u>resonance structures</u>. (Figure 1), on these structures, we will obtain a n<u>egative charge on carbon 2</u> in the pyrrole ring, therefore on this carbon we can generate an attack to an electrophile.
The second step is to check how the mechanism take place. An <u>electrophile is generated</u> by the 
and 
. This electrophile can be <u>attacked</u> by the negative charge on carbon 2 producing the 2-bromopyrrole. (See figure 2).
I hope it helps!
