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WARRIOR [948]
3 years ago
15

If 3.0×105 j of heat are added to the ice, what is the final temperature of the system?

Chemistry
1 answer:
lara [203]3 years ago
3 0
A wet-chemistry biochemical analyzer<span> was assessed for in-practice veterinary use. Its small size may mean a cost-effective method for low-throughput in-house biochemical analyses for first-opinion practice. The objectives of our study were to determine imprecision, total observed error, and acceptability of the </span>analyzer<span> for measurement of common canine and feline </span>serum<span> analytes, and to compare clinical </span>sample<span> results to those from a commercial reference </span>analyzer<span>. Imprecision was determined by within- and between-run repeatability for canine and feline pooled </span>samples<span>, and manufacturer-supplied quality control material (QCM). Total observed error (TEobs) was determined for pooled </span>samples<span> and QCM. Performance was assessed for canine and feline pooled </span>samples<span> by sigma metric determination. Agreement and errors between the in-practice and reference </span>analyzers<span> were determined for canine and feline clinical </span>samples<span> by Bland-Altman and Deming regression analyses. Within- and between-run precision was high for most analytes, and TEobs(%) was mostly lower than total allowable error. Performance based on sigma metrics was good (σ > 4) for many analytes and marginal (σ > 3) for most of the remainder. Correlation between the </span>analyzers<span> was very high for most canine analytes and high for most feline analytes. Between-</span>analyzer<span> bias was generally attributed to high constant error. The in-practice </span>analyzer<span> showed good overall performance, with only calcium and phosphate analyses identified as significantly problematic. Agreement for most analytes was insufficient for transposition of reference intervals, and we recommend that in-practice-specific reference intervals be established in the laboratory.</span>
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The active ingredient in aspirin is acetylsalicylic acid. A 2.79 g sample of acetylsalicylic acid required 30.15 mL of 0.5137 M
vivado [14]

Answer:

Molar mass = 180 g/mol

Ka = 3.31x10⁻⁴

Explanation:

Because the acetylsalicylic is a monoprotic acid, it only leaves 1 mol of H⁺ in the reaction, so, it's necessary 1 mol of NaOH for each 1 mol of acetylsalicylic acid. The number of moles of NaOH is the volume, in L, multiplied by the concentration:

n = 0.03015*0.5137 = 0.01549

Which is also the number of moles of the acid. The molar mass is the mass, in g, divided by the number of moles:

M = 2.79/0.01549

M = 180 g/mol

After reacting with the base, the conjugate base of the acid will be formed, and the equilibrium between the acid form (HA) and the conjugate base (A⁻) is a buffer. It formed 0.01549 moles of A⁻, which will react with the moles of H⁺ from HCl to form HA.

nH⁺ = nHCl = 0.01741*0.448 = 0.0078 mol

A⁻           +       H⁺            ⇄   HA

0.01549     0.0078                 0        Initial

-0.0078     -0.0078         +0.0078   Reacts

0.0078            0                0.0078   Equilibrium

For a buffer, the pH can be calculated by the Handerson-Halsebach equation:

pH = pKa + log[A⁻]/[HA]

Because the volume is the same, we can use the number of moles instead of the concentration:

3.48 = pKa + log(0.0078/0.0078)

pKa = 3.48

pKa = -logKa

Ka = 10^{-pKa}

Ka = 10^{-3.48}

Ka = 3.31x10⁻⁴

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Explanation:

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Answer:

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mass number remains constant while atomic number has been increased by 1 unit . beta is electron like element where its mass number is 0 and atomic number is -1.

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Explanation: Water, CO2, and table salt are compounds. They are composed of two or more separate elements; a mixture, where as gold is neither.

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