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goldfiish [28.3K]
3 years ago
15

Which area is MOST likely to support a marsh ecosystem? a sunny, open area with lots of sand dunes a shallow, sheltered area nea

r an estuary a rocky, coastal area with very high tides deep ocean water miles from a river's mouth
Chemistry
2 answers:
Vedmedyk [2.9K]3 years ago
7 0

Answer:

coastal area with very high tides deep ocean water miles from a river's mouth

Explanation:

Marshes are a type of wetland ecosystem where water covers the ground for long periods of time. Marshes are dominated by herbaceous plants, such as grasses, reeds, and sedges(National Geographic Society).

Animals found in a marsh include;  frogs, toads, turtles, snakes, mammals, birds and insects. A marsh is a wetland that is dominated by herbaceous rather than woody plant species(Wikipedia). It is characterized by very high tides deep ocean water miles from a river's mouth.

irga5000 [103]3 years ago
6 0

Answer:

i also need help with this question

Explanation:

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How many atoms are<br> below?<br> C6H1206
Vinvika [58]

Answer:

24 atoms

Explanation:

6 Carbon atoms

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Which is the top layer of groundwater?
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Answer:

An aquifer is a layer of porous substrate that contains and transmits groundwater. ... The upper level of this saturated layer of an unconfined aquifer is called the water table or phreatic surface. Below the water table, where in general all pore spaces are saturated with water, is the phreatic zone.

4 0
3 years ago
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What is the difference between mass number and atomic number?
astra-53 [7]

Answer:

They are found the same way but use different symbols when found.

Explanation:

3 0
3 years ago
A zinc rod is placed in 0.1 MZnSO4 solution at 298 K. Write the electrode reaction and calculate the potential of the electrode.
yanalaym [24]

<u>Answer:</u> The potential of electrode is -0.79 V

<u>Explanation:</u>

When zinc is dipped in zinc sulfate solution, the electrode formed is Zn^{2+}(aq.)/Zn(s)

Reduction reaction follows:  Zn^{2+}(0.1M)+2e^-\rightarrow Zn(s);(E^o_{Zn^{2+}/Zn}=-0.76V)

To calculate the potential of electrode, we use the equation given by Nernst equation:

E_{(Zn^{2+}/Zn)}=E^o_{(Zn^{2+}/Zn)}-\frac{0.059}{n}\log \frac{[Zn]}{[Zn^{2+}]}

where,

E_{cell} = electrode potential of the cell = ?V

E^o_{cell} = standard electrode potential of the cell = -0.76 V

n = number of electrons exchanged = 2

[Zn]=1M    (concentration of pure solids are taken as 1)

[Zn^{2+}]=0.1M

Putting values in above equation, we get:

E_{cell}=-0.76-\frac{0.059}{2}\times \log(\frac{1}{0.1})\\\\E_{cell}=-0.79V

Hence, the potential of electrode is -0.79 V

4 0
3 years ago
A. The reactant concentration in a zero-order reaction was 8.00×10−2 M after 155s and 3.00×10−2 M after 355s . What is the rate
irga5000 [103]

Answer:

A) The rate constant is 2.50 × 10⁻⁴ M/s.

B) The initial concentration of the reactant is 11.9 × 10⁻² M.

C) The rate constant is 0.0525 s⁻¹

D) The rate constant is 0.0294 M⁻¹ s⁻¹

Explanation:

Hi there!

A) The equation for a zero-order reaction is the following:

[A] = -kt + [A₀]

Where:

[A] = concentrationo f reactant A at time t.

[A₀] = initial concentration of reactant A.

t = time.

k = rate constant.

We know that at t = 155 s, [A] = 8.00 × 10⁻² M and at t = 355 s [A] = 3.00 × 10⁻² M. Then:

8.00 × 10⁻² M = -k (155 s) +  [A₀]

3.00 × 10⁻² M = -k (355 s) + [A₀]

We have a system of 2 equations with 2 unknowns, let´s solve it!

Let´s solve the first equation for [A₀]:

8.00 × 10⁻² M = -k (155 s) +  [A₀]

8.00 × 10⁻² M + 155 s · k = [A₀]

Replacing [A₀] in the second equation:

3.00 × 10⁻² M = -k (355 s) + [A₀]

3.00 × 10⁻² M = -k (355 s) + 8.00 × 10⁻² M + 155 s · k

3.00 × 10⁻² M - 8.00 × 10⁻² M = -355 s · k + 155 s · k

-5.00 × 10⁻² M = -200 s · k

-5.00 × 10⁻² M/ -200 s = k

k = 2.50 × 10⁻⁴ M/s

The rate constant is 2.50 × 10⁻⁴ M/s

B) The initial reactant conentration will be:

8.00 × 10⁻² M + 155 s · k = [A₀]

8.00 × 10⁻² M + 155 s · 2.50 × 10⁻⁴ M/s = [A₀]

[A₀] = 11.9 × 10⁻² M

The initial concentration of the reactant is 11.9 × 10⁻² M

C) In this case, the equation is the following:

ln[A] = -kt + ln([A₀])

Then:

ln(7.60 × 10⁻² M) = -35.0 s · k + ln([A₀])

ln(5.50 × 10⁻³ M) = -85.0 s · k + ln([A₀])

Let´s solve the first equation for ln([A₀]) and replace it in the second equation:

ln(7.60 × 10⁻² M) = -35.0 s · k + ln([A₀])

ln(7.60 × 10⁻² M) + 35.0 s · k = ln([A₀]

Replacing ln([A₀]) in the second equation:

ln(5.50 × 10⁻³ M) = -85.0 s · k + ln([A₀])

ln(5.50 × 10⁻³ M) = -85.0 s · k + ln(7.60 × 10⁻² M) + 35.0 s · k

ln(5.50 × 10⁻³ M) -  ln(7.60 × 10⁻² M) = -85.0 s · k + 35.0 s · k

ln(5.50 × 10⁻³ M) -  ln(7.60 × 10⁻² M) = -50.0 s · k

(ln(5.50 × 10⁻³ M) -  ln(7.60 × 10⁻² M)) / -50.0 s = k

k = 0.0525 s⁻¹

The rate constant is 0.0525 s⁻¹

D) In a second order reaction, the equation is as follows:

1/[A] = 1/[A₀] + kt

Then, we have the following system of equations:

1/ 0.510 M = 1/[A₀] + 205 s · k

1/5.10 × 10⁻² M = 1/[A₀] + 805 s · k

Let´s solve the first equation for 1/[A₀]:

1/ 0.510 M = 1/[A₀] + 205 s · k

1/ 0.510 M - 205 s · k = 1/[A₀]

Now let´s replace 1/[A₀] in the second equation:

1/5.10 × 10⁻² M = 1/[A₀] + 805 s · k

1/5.10 × 10⁻² M = 1/ 0.510 M - 205 s · k + 805 s · k

1/5.10 × 10⁻² M - 1/ 0.510 M = - 205 s · k + 805 s · k

1/5.10 × 10⁻² M - 1/ 0.510 M = 600 s · k

(1/5.10 × 10⁻² M - 1/ 0.510 M)/ 600 s = k

k = 0.0294 M⁻¹ s⁻¹

The rate constant is 0.0294 M⁻¹ s⁻¹

8 0
4 years ago
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