Not sure what to do can you help

HELP ME OMG WHY IS NOBODY HELPING ME SJCNEOVKRM

Sholpan [36]

I believe it would be CS and GE (option 3). i hope i helped ya out.

3 0

4 years ago

Help please !

AURORKA [14]

Answer:

false

true

Explanation:

false - changing the hypothesis to meet your needs is not a good researcher

true - when you can further analyze and explain then you have a successful experiment even if it's not what you expected

true - successful experiments do not end there. they can lead to more in depth questions.

8 0

3 years ago

Which sentence describes the bond formed between two identical atoms?

Lilit [14]

The best answer is C

Since identical atoms would have the same electronegativity, thus making its electronegativity difference close to zero, if not equal to zero (O), making the bond between the two to be covalent. Thus, a chemical bond formed between two identical atoms is a covalent bond.

3 0

3 years ago

Read 2 more answers

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

Lue Arg Lys Arg Met Phe Arg Ser

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

Lue __ __ __ __ __ __ Ser

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

Lue __ __ __ Met __ __ Ser

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

Lue __ __ __ Met Phe Arg Ser

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

Lue Arg Lys Arg Met Phe Arg Ser

4 0

4 years ago

/10

ddd [48]

Explanation:

Uranium-238 undergoes a radioactive decay series consisting of 14 separate steps before producing stable lead-206. This series consists of eight α decays and six β decays.

6 0

3 years ago