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yawa3891 [41]
3 years ago
7

A. What chemicals are involved in the formation of acid rain? What are the sources of these chemicals? (2 points)

Chemistry
1 answer:
lesya692 [45]3 years ago
6 0

Answer:

See explanation

Explanation:

The to main chemicals that lead to acid rain are SOx and NOx. The major source of oxides of sulphur are power plants while the major source of oxides of nitrogen is the combustion of fossil fuels.

B. There are two types of acid rain; wet and dry. Wet type acid rain occurs when NOx and SOx combine with water vapour in the atmosphere and fall as precipitation while in dry type, wind deposits these acidic gases/matter on the surfaces of buildings, cars, trees etc. Rain water washes off these acidic deposits and the runoff is more acidic than the rain water.

C. Natural rain water has a pH of about 5.5 due to the fact that water dissolve CO2 in the atmosphere. This means that natural rain water is also slightly acidic. Rain water that dissolves SOx or NOx is often more acidic than these hence the term 'enhanced acid rain' may be used.

Again, since precipitation could be solid or liquid, the term 'acid deposition' is better.

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Question 1 (2 points)
bogdanovich [222]

Answer:

3.75 L

Explanation:

We can solve this problem by using <em>Charles' law</em>, which states:

  • V₁T₂=V₂T₁

Where subscript 1 stands for initial volume and temperature and subscript 2 for final volume and temperature, meaning that in this case:

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We <u>input the data</u>:

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5 0
3 years ago
Determine the primary structure of an octapeptide from the following data: acid-catalyzed hydrolysis gives 2 arg, leu, lys, met,
erma4kov [3.2K]

Complete Question

The complete question is shown on the first uploaded image

Answer:

The sequence of these amino acid would be

          <u>Lue</u>  <u>Arg</u>  <u>Lys</u>  <u>Arg</u>  <u>Met</u>  <u>Phe</u> <u>Arg</u>  <u>Ser</u>

Explanation:

The acid-catalyzed hydrolysis from makes us to understand that the  polypeptides contains 8 amino acids

   From the question we are told that the Edman's reagent releases Leu it means that the N-terminal amino acid would be Lue(i.e Leucine)

     Also from the question we are told that the Carboxypeptidase  released Ser this mean the the C-terminal  amino acid would be Ser ( i.e Serine)

   The Amino acids would in the polypeptides would be arranged like this  

         

         <u>Lue</u> __  __  __  __  __ __  <u>Ser</u>

Now from the question we are told that treatment with cranogen bromide form two peptides.

   Now generally  cranogen bromide divides a peptide on  the C- side(i.e the extreme left side ) of  Met(Methionine)(This is an amino acid obtained by hydrolysis of most common peptides )

   So this means that any peptides  containing Met(Methionine) must have Methionine as a C- terminal amino acid(i.e at extreme left) and for peptides that does not contain Met must be C - terminal peptides

From the question we see that it is the second peptide that contain Met and it is a penta peptide(i.e it contains 5 amino acid)  

    Thus the fifth amino acid is  Met  

So the sequence of these amino acid would now be  

          <u>Lue</u> __  __  __  <u>Met</u>  __ __  <u>Ser</u>

From the question we are told that the the Trypsin-catalyzed hydrolysis forms two amino acid and two peptides  

   Now generally Trypsin divides a peptide  on the  C- side(i.e the extreme left) of Arg(Arginine) and Lys (lysine) and any peptide that holds Arg or Lys  must have them as their C- terminal  amino acids

   From the first peptide in the two peptide formed we see that  Arg would be the Seventh amino acid of the octapeptide because commonly the trypsin that sticks to the C-side of Arg would for Ser

and Phe would be the sixth amino acid of the octapeptide

So the sequence of these amino acid would be

       <u>Lue</u> __  __  __  <u>Met</u>  <u>Phe</u> <u>Arg</u>  <u>Ser</u>

Looking  at the first amino acid formed from the Trypsin-catalyzed hydrolysis  we see that Arg would be the fourth amino acid of  octapeptide      as Trypsin divides a peptide  on the  C- side(i.e the extreme left) of Arg(Arginine).

From the second peptide of the  Trypsin-catalyzed hydrolysis  we see that Lys would be the third amino acid of the octapeptide as trypsin divides on the  C- side of  Lys (lysine) and Tyr would be the second amino acid of the octapeptide

So the sequence of these amino acid would be

          <u>Lue</u>  <u>Arg</u>  <u>Lys</u>  <u>Arg</u>  <u>Met</u>  <u>Phe</u> <u>Arg</u>  <u>Ser</u>

           

4 0
3 years ago
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