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victus00 [196]
3 years ago
9

7. What are the coefficients needed to balance the following chemical equation?

Chemistry
1 answer:
Allisa [31]3 years ago
7 0

Answer:

D, 2,2,3,

Explanation:

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Hi! help me please. CALCULATE THE NUMBER OF MOLECULES FOUND IN 8 MOL OF WATER?
kvasek [131]

Answer:

so the number of molecules in 8 moles of water is 4.8176×10^24

Explanation:

number of moles=8moles

avogadro's number=6.022×10²³

number of molecules=?

as we know that

number of moles=\frac{number of molecules}{avogadro's number}

substituting the equation

number of moles × avogdro's number=number of molecules

number of molecules=8moles×6.022×10²³

number of molecules=4.8176×10^24

i hope this will help you :)

4 0
3 years ago
Bromo-4-fluorohexane has two chiral carbon atoms; therefore, the maximum number of possible stereoisomers that can be formed is
Zepler [3.9K]

Here we have to draw the four isomers of the compound 3-bromo-4-fluorohexane.

The four isomers of the compound is shown in the figure.      

In an organic molecule the chiral -C center is that where four (4) different groups are present. In 3-bromo-4-fluorohexane the 3 and 4 positions are chiral centers. The possible isomers of a molecule can be obtained from the formula 2n. As here 2 chiral centers are present thus number of stereoisomers will be 2×2 = 4.

The four different isomers as shown in the figure are 3R-, 4R-; 3S-, 4S; 3R, 4S and 3S-, 4R- 3-bromo-4-fluorohexane.

In the 3-bromo-4-fluorohexane the functional groups are -Br, C₂H₅, -C₃H₆F and -H for 3-position and -F, -C₂H₅, -C₃H₆ and -H for 4-position respectively.

The priority of the -3 position will be Br > C₃H₆F > C₂H₅ > H and for -4 position F > C₃H₆Br > C₂H₅ > H. If the rotation from the higher priority group to lower is clockwise and anticlockwise then the S- and R- notation are used respectively. However if the -H atom is present at the horizontal position then the notation will be reverse.

Thus the four isomers of the compound is shown.      

4 0
3 years ago
By what mechanism does cyclohexanol react when treated in sulfuric acid and what compound results?A) E 1; methoxycyclohexane B)
tensa zangetsu [6.8K]

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.

8 0
3 years ago
The material the start all reactions are ______ and the materials that are formed are called _____.
max2010maxim [7]

Answer:

I think the second space is chemical bonds

7 0
3 years ago
Read 2 more answers
If you are studying cells and heredity bwhat classes are u in
ValentinkaMS [17]
Probably life science or biology.
3 0
3 years ago
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