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iren [92.7K]
3 years ago
9

1. The sun's atmosphere is the ...........

Chemistry
1 answer:
Marrrta [24]3 years ago
8 0

Answer:

photosphere

Explanation:

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Bases turn litmus paper what color?<br><br> a) red<br> b) blue<br> c) yellow<br> d) pink
yKpoI14uk [10]
Answer:
blue
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5 0
3 years ago
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Calculate the vapor pressure at 35ºC of a solution made by dissolving 20.2 g of sucrose (C12H22O11)in 60.5 g of water. The vapor
sukhopar [10]

Answer:

P' = 41.4 mmHg → Vapor pressure of solution

Explanation:

ΔP = P° . Xm

ΔP = Vapor pressure of pure solvent (P°) - Vapor pressure of solution (P')

Xm = Mole fraction for solute (Moles of solvent /Total moles)

Firstly we determine the mole fraction of solute.

Moles of solute → Mass . 1 mol / molar mass

20.2 g . 1 mol / 342 g = 0.0590 mol

Moles of solvent → Mass . 1mol / molar mass

60.5 g . 1 mol/ 18 g = 3.36 mol

Total moles = 3.36 mol + 0.0590 mol = 3.419 moles

Xm = 0.0590 mol / 3.419 moles → 0.0172

Let's replace the data in the formula

42.2 mmHg - P' = 42.2 mmHg . 0.0172

P' = - (42.2 mmHg . 0.0172 - 42.2 mmHg)

P' = 41.4 mmHg

5 0
3 years ago
If electrons were used in the two-slit experiment instead of light, what change would need to be made to the slit spacing in ord
Andrei [34K]
In order to conduct the two-slit experiment with a beam of electrons, the slit opening has to be smaller than the opening for the light waves. This is because the wavelength of the electron beam is lower, which means it will pass through the large slit without diffracting. Diffraction will occur if the spacing is reduced. The reason that electrons have a smaller wavelength is because they have a higher energy than light waves.
5 0
3 years ago
If the solvent in a solution is water, the solution is
BlackZzzverrR [31]

Answer:

I don't know

Explanation:

Yet but I will find it for you

7 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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