<u>Given:</u>
Volume of HCl = 150 ml
Molarity of HCl = 0.10 M
<u>To determine:</u>
The # moles of HCl
<u>Explanation:</u>
The molarity of a solution is the number of moles of a solute dissolved in a given volume
In this case:
Molarity of HCl = moles of HCl/volume of the solution
moles of HCl = Molarity * volume = 0.10 moles.L-1 * 0.150 L = 0.015 moles
Ans: A)
Moles of HCl is 0.015
Answer:
(BH3 follows the octet rule by dimerizing, as Hadi Kurniawan AR pointed out.) For H and He, an "octet" = 2 electrons. Boron does prefer to follow the octet rule, in that it likes to form borate compounds such as NaBH4. It also is happy to form compounds with elements with lone pairs.
From the equation of the reaction; for every 1 mole of copper, the reaction uses 2 moles of silver nitrate.
<h3>What is a reaction?</h3>
A chemical reaction involves the transformation of one chemical specie into another. The reaction is not shown here hence the question is incomplete.
However, the reaction should be of the sort; Cu + 2AgNO3 ---> Cu(NO3)2 + Cu. Thus, for every 1 mole of copper, the reaction uses 2 moles of silver nitrate.
Learn more about chemical reaction: brainly.com/question/6876669
Answer:
The boiling point is 308.27 K (35.27°C)
Explanation:
The chemical reaction for the boiling of titanium tetrachloride is shown below:
Ti
⇒ Ti
ΔH°
(Ti
) = -804.2 kJ/mol
ΔH°
(Ti
) = -763.2 kJ/mol
Therefore,
ΔH°
= ΔH°
(Ti
) - ΔH°
(Ti
) = -763.2 - (-804.2) = 41 kJ/mol = 41000 J/mol
Similarly,
s°(Ti
) = 221.9 J/(mol*K)
s°(Ti
) = 354.9 J/(mol*K)
Therefore,
s° = s° (Ti
) - s°(Ti
) = 354.9 - 221.9 = 133 J/(mol*K)
Thus, T = ΔH°
/s° = [41000 J/mol]/[133 J/(mol*K)] = 308. 27 K or 35.27°C
Therefore, the boiling point of titanium tetrachloride is 308.27 K or 35.27°C.
Answer:
See attachment.
Explanation:
In the first step, a cyclic structure with a positive bromine is formed. The bromine shares the positive charge with the two carbons that it is bonded to, so the carbons are partially positive.
The second bromine atom then attacks the carbon center, coming in from below the first bromine atom ("backside attack") where the antibonding orbital of the second bromine atom is.
The stereochemistry of the mechanism causes the final product to be an anti-dibromocyclohexane.