Answer:
116g/mol
Explanation:
Mg=24
NO2=46
multiple 46 by 2and then add 24
Answer:
Coefficient in front of the 
in the balanced equation - 1
Explanation:
The unbalanced Chemical equation is shown below as:-
On the left hand side,
There are 1 boron atom and 3 fluorine atoms and 1 sodium and hydrogen atoms.
On the right hand side,
There are 2 boron atoms and 6 hydrogen atoms and 1 sodium and fluorine atoms.
Thus,
leftside, 
must be multiplied by 2 to balance boron and right side, 
must be multiplied by 6 to balance fluorine. Left side, 
must be multiplied by 6 to balance sodium and hydrogen atoms.
Thus, the balanced reaction is:-
<u>Coefficient in front of the in the balanced equation - 1</u>
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Gene cloning: copies a few segments of DNA or genes.
Reproductive cloning: it copies the whole animal.
Therapeutic cloning: produces embryonic stem cells for experiments aimed at creating tissues to replace injured or diseased tissues.
Answer:
[NaOH} = 0.4 M
Explanation:
In a reaction of neutralization, we determine the equivalence point of the titration. In this case, we have a strong base and a strong acid.
(H₂SO₄, is considered strong, but the first deprotonation is weak)
2NaOH + H₂SO₄ → Na₂SO₄ + 2H₂O
As we have 2 protons in the acid, we need 2 OH⁻ from the base to form 2 molecules of water.
In the equivalence point we know mmoles of base = mmoles of acid
Let's finish the excersise with the formula
25 mL . M NaOH = 28.2 mL . 0.355M
M NaOH = (28.2 mL . 0.355M) / 25 mL → 0.400
Answer:
E 1: cyclohexene
Explanation:
This reaction is an example of the dehydration of cyclic alcohols. The reaction proceeds in the following steps;
1) The first step of the process is the protonation of the cyclohexanol by the acid. This now yields H2O^+ attached to the cyclohexane ring.
2) the water molecule, which a good leaving group now leaves yielding a carbocation. This now leaves a cyclohexane carbocation which is highly reactive.
3) A water molecule now abstracts a proton from the carbon adjacent to the carbocation leading to the formation of cyclohexene and the regeneration of the acid catalyst. This is an E1 mechanism because it proceeds via a carbocation intermediate and not a concerted transition state, hence the answer.
