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GuDViN [60]
3 years ago
9

This atom can form up to _____ single covalent bond(s). An atom with two electron shells. There is one electron pair in the inne

r electron shell and four unpaired electrons in the outer electron shell.
Chemistry
1 answer:
Deffense [45]3 years ago
3 0

Answer:

Explanati4 ELECTRONS ARE IN THE OUTERMOST SHELL

on:

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2. Water is an example of a(n)
Alexus [3.1K]

it would be A ,inorganic Compound

6 0
3 years ago
Consider the synthesis of ammonia 3 H2+ N2 à 2 NH3 If a student were to react 38.5 g of nitrogen gas, how many moles of ammonia
Wittaler [7]

Answer:

2.75 mol

Explanation:

Given data:

Mass of Nitrogen = 38.5 g

Moles of ammonia produced = ?

Solution:

Chemical  equation:

N₂ + 3H₂    →     2NH₃

Number of moles of nitrogen:

Number of moles = mass/ molar mass

Number of moles = 38.5 g/ 28 g/mol

Number of moles = 1.375 mol

Now we will compare the moles of ammonia and nitrogen from balance chemical equation.

           N₂            :            NH₃

            1              :             2

           1.375       :           2×1.375 = 2.75 mol

Thus 2.75 moles of ammonia  are produced from 38.5 g of nitrogen.

4 0
3 years ago
What is the percent composition of Br in CuBr3?
tekilochka [14]

Answer:

about 79% (79.04369332 to be exact)

Explanation:

Percent composition=(Molar mass of element x amount of it)/Molar mass of compound x 100

Br= 3 x 79.9/303.25 x100=79.04369332

6 0
3 years ago
Which graph correctly shows the effect on the freezing point caused by increasing the molality of a solution ?
beks73 [17]
The answer to your question is graph A :)
6 0
3 years ago
Read 2 more answers
Which of the following two combinations of reactants is more appropriate for the preparation of p-nitrophenyl phenyl ether? Fluo
VladimirAG [237]

Answer:

p-fluoronitrobenzene and sodium phenoxide is more appropriate

Explanation:

An ipso substitution is required to form p-nitrophenyl phenyl ether.

For this ipso substitution, an alkoxide anion needs to attack as a nucleophile at the carbon atom attached to fluorine atom and thereby substitute that F atom.

p-nitrophenoxide is an weak nucleophile as compared to phenoxide due to presence of electron withdrawing resonating effect of nitro group at para position.

p-fluoronitrobenzene is a good choice for nucleophilic attack by alkoxide anion as compared to fluorobenzene due to higher positive charge density at carbon atom directly attached to F atom. Higher positive charge density arises due to presence of electron withdrawing resonating effect og nitro group at para position.

So, p-fluoronitrobenzene and sodium phenoxide is more appropriate

5 0
3 years ago
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