Complete Question:
A chemist prepares a solution of silver (I) perchlorate (AgCIO4) by measuring out 134.g of silver (I) perchlorate into a 50.ml volumetric flask and filling the flask to the mark with water. Calculate the concentration in mol/L of the silver (I) perchlorate solution. Round your answer to 2 significant digits.
Answer:
13 mol/L
Explanation:
The concentration in mol/L is the molarity of the solution and indicates how much moles have in 1 L of it. So, the molarity (M) is the number of moles (n) divided by the volume (V) in L:
M = n/V
The number of moles is the mass (m) divided by the molar mass (MM). The molar mass of silver(I) perchlorate is 207.319 g/mol, so:
n = 134/207.319
n = 0.646 mol
So, for a volume of 50 mL (0.05 L), the concentration is:
M = 0.646/0.05
M = 12.92 mol/L
Rounded to 2 significant digits, M = 13 mol/L
Answer:
The answer to your question is below
Explanation:
11. Alkali metals
12. Halogens
13. Transition metals
14. Halogens
15. Noble gases
16. Alkaline earth metals
17. Transition metals
18. Alkaline earth metals
19. Transition metals
20. Alkali metals
21.- Periods
22.- Calcium
23.- Iodine, I
24.- A. atomic number
Caffeine has the following percent composition: carbon 49.48%, hydrogen 5.19%, oxygen 16.48% and nitrogen 28.85%. Its molecular weight is 194.19 g/mol.
The balanced equation for the given reaction:
C₆H₁₂O₆ (glucose) + 6O₂→ 6CO₂ + 6H₂O
So in the balanced equation the coefficients before glucose, oxygen, water and carbon dioxide are 1, 6, 6 and 6 respectively.
Therefore, the sum of the coefficients in the balanced equation
= 1 + 6 + 6 + 6
= 19
The correct answer is 19.
<h3><u>Full Question:</u></h3>
The following compound has been found effective in treating pain and inflammation (J. Med. Chem. 2007, 4222). Which sequence correctly ranks each carbonyl group in order of increasing reactivity toward nucleophilic addition?
A) 1 < 2 < 3
B) 2 < 3 < 1
C) 3 < 1 < 2
D) 1 < 3 < 2
<h3><u>Answer: </u></h3>
The rate of nucleophilic attack of carbonyl compounds is 2<3 <1.
Option B
<h3><u>Explanation. </u></h3>
Nucleophilic attack is explained as the attack of an electron rich radical to a carbonyl compound like aldehyde or a ketone. A nucleophile has a high electron density, so it searches for a electropositive atom where it can donate a portion of its electron density and become stable.
A carbonyl compound is a 
hybridized carbon atom with a double bonded oxygen atom in it. The oxygen atom pulls a huge portion of electron density from carbon being very electropositive.
In a ketone, there are two factors that make it less likely to undergo a nucleophilic attack than aldehyde. Firstly, the steric hindrance of two carbon groups being attached with the carbonyl carbon makes it harder for the nucleophile to approach. Secondly, the electron push by the carbon groups attached makes the carbonyl carbon a bit less electropositive than the aldehyde one. So aldehydes are more reactive towards a nucleophilic addition reaction.
