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saveliy_v [14]
3 years ago
10

An animal cell has a 0.9% saline environment is placed into a solution that is 9% saline. What will happen to the cell

Chemistry
1 answer:
Softa [21]3 years ago
7 0

The concentration of cell is less than that of the solution .

Hence the cell will be called as hypotonic and the solution will be called as hypertonic.

in order to balance the concentration on the two sides of cell (inside and outside in the solution) there will be movement of solvent particles (through semipermeable membrane ) from cell (lower concentration of solute) to solution (higher concentration of solute).

Thus cell will shrink.



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What is the coefficient of Ca(OH)2 in the equation Ca(OH)2 + HNO3 → Ca(NO3)2 + H2O when balanced using the smallest possible coe
Vikentia [17]

Answer:

The coefficient of Ca(OH)2 is 1

Explanation:

Step 1: unbalanced equation

Ca(OH)2 + HNO3 → Ca(NO3)2 + H2O

Step 2: Balancing the equation

On the right side we have 2x N (in Ca(NO3)2 ) and 1x N on the left side (in HNO3). To balance the amount of N on both sides, we have to multiply HNO3 by 2.

Ca(OH)2 + 2HNO3 → Ca(NO3)2 + H2O

On the left side we have 4x H (2xH in Ca(OH)2 and 2x H in HNO3), on the right side we have 2x H (in H2O). To balance the amount of H on both sides, we have to multiply H2O on the right side, by 2.

Now the equationis balanced.

Ca(OH)2 + 2HNO3 = Ca(NO3)2 + 2H2O

The coefficient of Ca(OH)2 is 1

4 0
3 years ago
Both 1,2−dihydronaphthalene and 1,4−dihydronaphthalene may be selectively hydrogenated to 1,2,3,4−tetrahydronaphthalene. One of
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Answer:

1,4-dihydro = 113 kJ·mol⁻¹

1,2-dihydro = 101 kJ·mol⁻¹

Explanation:

In 1,4-dihydronaphthalene, the 2,3-double bond is isolated from the benzene ring.

In 1,2-dihydronaphthalene, the 3,4-double bond is conjugated with the benzene ring.

Thus, 1,2-dihydronaphthalene is partially stabilized by resonance interactions between the ring and the double bond (think, styrene).

1,2-Dihydronaphthalene is at a lower energy level because of this stabilization.

The heat of hydrogenation of 1,2-dihydronaphthalene is therefore less than that of the 1,4-isomer when each is hydrogenated to the common product, 1,2,3,4-tetrahydronaphthalene.

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