Answer:
Covalent bonds.
Explanation:
Diamond is organized in a giant lattice structure with strong covalent bonds between carbon atoms. Each carbon atom forms 4 bonds. Explanation: Each carbon atom has four electrons in its outer shell, all of which form covalent bonds that are strong and hard to break.
Answer:
0.1066 hours
Explanation:
A common pesticide degrades in a first-order process with a rate constant (k) of 6.5 1/hours. We can calculate its half-life (t1/2), that is, the times that it takes for its concentration to be halved, using the following expression.
t1/2 = ln2/k
t1/2 = ln2/6.5 h⁻¹
t1/2 = 0.1066 h
The half-life of the pesticide is 0.1066 hours.
The reaction, as what is depicted in the thermonuclear equation is one of the best example of an endothermic reaction. In addition, the endothermic process revolves around the idea that the system can also absorb the energy from its surroundings, in contrast to the idea of releasing its energy to its environment.
Answer:
Pb: 22.4 at%
Sn: 77.6 at%
Explanation:
It is possible to find at% of Pb and Sn converting mass in moles using molar mass assuming a basis of 100g, thus:
Pb: 33.5g × (1mol / 207.2g) = <em>0.1617mol</em>
Sn: 66.5g × (1mol / 118.7g) = <em>0.5602mol</em>
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Total moles: 0.1617mol + 0.5602mol = 0.7219mol
Composition in at%:
Pb: 0.1617mol / 0.7219mol × 100 = <em>22.4 at%</em>
Sn: 0.5602mol / 0.7219mol × 100 = <em>77.6 at%</em>
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Although phlorizin inhibition of Na+-glucose cotransport occurs within a few seconds, 3H-phlorizin binding to the sodium-coupled glucose transport protein(s) requires several minutes to reach equilibrium (the fast-acting slow-binding paradigm). Using kinetic models of arbitrary dimension that can be reduced to a two-state diagram according to Cha’s formalism, we show that three basic mechanisms of inhibitor binding can be identified whereby the inhibitor binding step either (A) represents, (B) precedes, or (C) follows the rate-limiting step in a binding reaction. We demonstrate that each of mechanisms A–C is associated with a set of unique kinetic properties, and that the time scale over which one may expect to observe mechanism C is conditioned by the turnover number of the catalytic cycle. In contrast, mechanisms A and B may be relevant to either fast-acting or slow-binding inhibitors.
Explanation:
