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algol [13]
2 years ago
6

3. 2 HCl (aq)

Chemistry
1 answer:
tekilochka [14]2 years ago
6 0

Explanation:

balance the equation ...HCl,Ba(OH) and BaCl2 are aqueous

know groups of the elements H 1+ ,Cl -,Ba 2+,OH-

write complete ionic eqution and eliminate spectator ions those appearing on both sides Cl and Ba

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Make the equations for the reactions between calcium and hydrochloric acid, name the products.
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Answer:

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Balance the folowing equation.<br> S + 02<br> ws<br> SO:
Rzqust [24]

Answer:

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Explanation:

i hope it will help u

6 0
3 years ago
Which of the following is an organic moleclue ?
Doss [256]

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6 0
3 years ago
If you have 16 g of manganese (II) nitrate tetrahydrate, how much water is required to prepare 0.16 M solution from this amount
Schach [20]

<u>Answer:</u> The amount of water required to prepare given amount of salt is 398.4 mL

<u>Explanation:</u>

To calculate the volume of solution, we use the equation used to calculate the molarity of solution:

\text{Molarity of the solution}=\frac{\text{Mass of solute}\times 1000}{\text{Molar mass of solute}\times \text{Volume of solution (in mL)}}

We are given:

Molarity of solution = 0.16 M

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Putting values in above equation, we get:

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Volume of water = Volume of solution = 398.4 mL

Hence, the amount of water required to prepare given amount of salt is 398.4 mL

4 0
3 years ago
In a two-step synthesis, C6H11Br is converted into C6H12O. From the structure of the product, molecular formula of the starting
tamaranim1 [39]

Answer:

See explanation below

Explanation:

The question is incomplete. However in picture 1, you have the starting materials and the structure of the product, which you miss in this part.

Now, in picture 2, you have the starting reactant and the product, and the mechanism that is taking place here.

First, all what we have here is an acid  base reaction. In the first step, we are using the acid medium to convert the reactant into an alcohol. The bromine there, is not leaving the molecule yet, because it's neccesary for the next step. The starting reactant is an alkene, in that way, we can convert the reactant in the first step into a secondary alcohol. In other words, the first reaction is a alkene hydration.

In the second step, we use a strong base. You may say this is a strong nucleophile and will do a Sn2 reaction to form another alcohol there, but it's not the case, because, before any kind of reaction happens, the priority here is always the acid base, so the base will react with the acidic hydrogen. In this case, it will substract an hydrogen from the OH. When this happens, the lone pair will do an auto condensation here, and attacks the bromine in the molecule. In this way, the molecule will become a cyclomolecule, and that way it form the final product.

See picture 2, for mechanism

8 0
3 years ago
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