Answer:
D.
Explanation:
Adding more gas particles to a set volume will increase the number of collisions, thus increasing collision force and pressure.
Answer:
ΔH = -470.4kJ
Explanation:
It is possible to sum 2 or more reactions to obtain the ΔH of the reaction you want to study (Hess's law). Using the reactions:
1. CaC2(s) + 2H2O(l) → C2H2(g) + Ca(OH)2(s)ΔH = −414kJ
2. 6C2H2(g) + 3CO2(g) + 4H2O(g) → 5CH2CHCO2H(g)ΔH = 132kJ
6 times the reaction 1.
6CaC2(s) + 12H2O(l) → 6C2H2(g) + 6Ca(OH)2(s)ΔH = −414kJ*6 = -2484kJ
This reaction + 2:
6CaC2(s) + 3CO2(g) + 16H2O(l) → + 6Ca(OH)2(s) + 5CH2CHCO2H(g) ΔH = -2484kJ + 132kJ = -2352kJ
As we want to calculate the net change enthalpy in the formation of just 1 mole of acrylic acid we need to divide this last reaction in 5:
6/5CaC2(s) + 3/5CO2(g) + 16/5H2O(l) → + 6/5Ca(OH)2(s) + CH2CHCO2H(g) ΔH = -2352kJ / 5
<h3>ΔH = -470.4kJ</h3>
Filter flasks are
also known as vacuum, suction or the Buchner flasks. They have thick walls and also
have a short glass tube. The thick walls are designed to enable the filter withstand
high pressures of vacuum applied to filter substances. Generally this is used
for filtering.
While the Erlenmeyer flask
also called as a conical flask, is a titration flask which consists of a
conical body, a flat bottom, and round neck. This is used for used for general
uses such as mixing, titrations, preparation of cultures, for
recrystallization, and for supporting filter funnels.
<span>Lastly, the Volumetric flasks are graduated flasks which having markings
for different volumes. They are calibrated accurately for a specific amount of
liquid that can be contained in it hence this is specially used for storing
precise amounts of liquid. </span>
What is the name of CuC2H3O2?
The answer is Copper (I) Acetate. (:
<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.
