It is known as its molar mass.
Answer:
Explanation:
In organic chemistry, the reaction between 2-butanol with TsCl and Et3N is known as the tosylation of the alcohol hydroxyl group. Alcohol is being changed to tosylate by the use of tosyl chloride under the influence of a base. Tosylation of alcohol is an example of a nucleophilic substitution reaction. From the image attached below, we will see how the reaction between 2-butanol proceed into the product by using tosyl chloride and a base(Et3N).
Answer:
Explanation:
you would have to look more around the page, for example look at some ways that you can right down.
<span>PbO
Let's look at each of the 4 compounds and see what's needed.
PbO.
* Oxygen has a valance shell that's missing 2 electrons and wants to get those 2 elections. Lead donates them, so you have a Lead (II) ions. This is a correct choice.
PbCl4
* Chlorine wants to grab 1 electron to fill it's valance shell and Lead donates that election. However, there's 4 chlorine atoms and every one of them wants and electron, and lead is donating all 4 of the desired electrons making the Lead (IV) ion. So this is a bad choice.
Pb2O
* Oxygen still wants 2 electrons and gets them from the lead. But there's 2 lead atoms and each of them donates 1 election making for 2 Lead(I) ions. So this too is a bad choice.
Pb2S
* Sulfur is in the same column of the periodic table as oxygen and if this compound were to exist would have similar properties as Pb2O and would have Lead(I) ions. So this is a bad choice.</span>
Answer:
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