Similar to Cohesion, adhesion is the attraction between molecules of different substances . Water uses adhesion when it's attraction to another substance is greater than the water's attraction to itself. if you have ever dropped a cup of water on a hardwood floor,you know that it spreads out instead of foaming beads.
I think the correct answer from the choices listed above is option A. The structural level of a protein least affected by a disruption in hydrogen bonding is the primary level. The other levels are very much affected by hydrogen bonding. Hope this answers the question.
Answer:
i mean kinda they should throw people in the air tho lol
Explanation:
Answer:
pH = 1.32
Explanation:
H₂M + KOH ------------------------ HM⁻ + H₂O + K⁺
This problem involves a weak diprotic acid which we can solve by realizing they amount to buffer solutions. In the first deprotonation if all the acid is not consumed we will have an equilibrium of a wak acid and its weak conjugate base. Lets see:
So first calculate the moles reacted and produced:
n H₂M = 0.864 g/mol x 1 mol/ 116.072 g = 0.074 mol H₂M
54 mL x 1L / 1000 mL x 0. 0.276 moles/L = 0.015 mol KOH
it is clear that the maleic acid will not be completely consumed, hence treat it as an equilibrium problem of a buffer solution.
moles H₂M left = 0.074 - 0.015 = 0.059
moles HM⁻ produced = 0.015
Using the Henderson - Hasselbach equation to solve for pH:
ph = pKₐ + log ( HM⁻/ HA) = 1.92 + log ( 0.015 / 0.059) = 1.325
Notes: In the HH equation we used the moles of the species since the volume is the same and they will cancel out in the quotient.
For polyprotic acids the second or third deprotonation contribution to the pH when there is still unreacted acid ( Maleic in this case) unreacted.
A(n )amide is an organic compound in which a carbonyl group is bonded to a nitrogen atom. This is <span>usually regarded as derivatives of carboxylic acids in which the hydroxyl group has been replaced by an amine or ammonia.</span>
