Answer:
bacteria
Explanation:
they are decomposers. they decompose dead material by fixing nitrogen
Answer:
1. d[H₂O₂]/dt = -6.6 × 10⁻³ mol·L⁻¹s⁻¹; d[H₂O]/dt = 6.6 × 10⁻³ mol·L⁻¹s⁻¹
2. 0.58 mol
Explanation:
1.Given ΔO₂/Δt…
2H₂O₂ ⟶ 2H₂O + O₂
-½d[H₂O₂]/dt = +½d[H₂O]/dt = d[O₂]/dt
d[H₂O₂]/dt = -2d[O₂]/dt = -2 × 3.3 × 10⁻³ mol·L⁻¹s⁻¹ = -6.6 × 10⁻³mol·L⁻¹s⁻¹
d[H₂O]/dt = 2d[O₂]/dt = 2 × 3.3 × 10⁻³ mol·L⁻¹s⁻¹ = 6.6 × 10⁻³mol·L⁻¹s⁻¹
2. Moles of O₂
(a) Initial moles of H₂O₂

(b) Final moles of H₂O₂
The concentration of H₂O₂ has dropped to 0.22 mol·L⁻¹.

(c) Moles of H₂O₂ reacted
Moles reacted = 1.5 mol - 0.33 mol = 1.17 mol
(d) Moles of O₂ formed

Small peak at 3000large peak at 1685F: it contains two benzene rings that is connected by a bunch of carbons and ketone-Explanation: The spectrum shows a stretching absorption consistent with a ketone functional group: carbonyl C=O stretching at ~1685 cm-1. (An aldehyde, by contrast, would also show a ~2700 cm-1 absorption for the carbonyl C-H stretch.) The C=O stretching frequency is consistent with an aromatic ketone, such as in compound F (1,4-diphenyl-1,4-butanedione). In contrast, an aliphatic ketone absorbs at higher energy (~1710 cm-1). The spectrum also shows the typical ~1600 & ~1500 cm-1 absorptions of a phenyl group.
Answer:
Due to the resonance structures
Explanation:
In the question:
"<em>Explain why, when the guanidino group of arginine is protonated, the double-bonded nitrogen is the nitrogen that accepts the proton. There is a scheme of a reversible reaction, where one equivalent of the reactant reacts with two equivalents of H plus</em>"
We have to take into account the structure of the <u>amino acid</u> arginine. In which, we have the amino and the carboxylic groups in the right and the <u>guanidine group in the left</u>.
In this group, we have a central carbon with three nitrogen atoms around and a double bond with the nitrogen on the top. This nitrogen on the top will accept the proton because the structure produced will have a positive charge on this nitrogen. Then, the double bond with the carbon can be delocalized into the nitrogen producing a positive charge in the carbon.
In this structure (<u>the carbocation</u>), we can have several resonance structures. In the <em>blue option</em>, we can produce a double bond with the nitrogen on the right. In the <em>purple option</em>, we can produce a double bond with the nitrogen on the left.
In conclusion, if the nitrogen in the top on the guanidine group accepts an hydrogen atom and we will have <u>several resonance structures that can stabilize the molecule.</u> Due to this, the nitrogen in the top its the best option to accept hydrogens.
See figure 1
I hope it helps!