Answer:
Why do we all not know the answer to this on the practical
Explanation:
Answer:
0!
Explanation:
- You need to search your pKa values for Asn (2.14, 8.75), Gly (2.35, 9.78) and Leu(2.33, 9.74), the first value corresponding to -COOH, the second to -NH3 (a third value would correspond to an R group, but in this case that does not apply), and we'll build a table to find the charges for your possible dissociated groups at indicated pH (7), we need to remember that having a pKa lower than the pH will give us a negative charge, having a pKa bigger than pH will give us a positive charge:
-COOH -NH3
pH 7------------------------------------------------------
Asn - +
Gly - +
Leu - +
- Now that we have our table we'll sketch our peptide's structure:
<em>HN-Asn-Gly-Leu-COOH</em>
This will allow us to see what groups will be free to react to the pH's value, and which groups are not reacting to pH because are forming the bond between amino acids. In this particular example only -NH group in Ans and -COOH in Leu are exposed to pH, we'll look for these charges in the table and add them to find the net charge:
+1 (HN-Asn)
-1 (Leu-COOH)
=0
The net charge is 0!
I hope you find this information useful and interesting! Good luck!
Answer:
They form when plates collide. I hope this helps you!
Free energy is the answer i hope this helped
Answer:

Explanation:
We must do the conversions
mass of C₆H₁₂O₆ ⟶ moles of C₆H₁₂O₆ ⟶ moles of O₂
We will need a chemical equation with masses and molar masses, so, let's gather all the information in one place.
Mᵣ: 180.16
C₆H₁₂O₆ + 6O₂ ⟶ 6CO₂ + 6H₂O
m/g: 18.1
(a) Moles of C₆H₁₂O₆

b) Moles of O₂