Answer:
It means the chemical entity is a radical
Explanation:
When we talk of unsaturation, we are referring to the number of pi-bonds in a chemical entity. The alkane, alkene and alkyne organic family are used to as common examples to explain the term unsaturation.
While alkynes have 3 bonds, it must be understood that they have 2 pi bonds only and as such their degree of saturation is two.
In the case of an alkene, there is only one single pi bond and as such the degree of unsaturation is 1.
Now in this case, we have a fractional 0.5 degree of unsaturation alongside the 3 to make a total of 3.5. So what’s the issue here?
The fractional part shows that the chemical entity we are dealing with here is a radical. While the integer 3 shows that there are 3 pi-bonds, the half pi bond remaining tells us that there is a missing electron on one of the atoms involved in the chemical bonding and as such, the 1/2 extra degree of unsaturation tends to tell us this.
Kindly recall that a radical is a chemical entity within which we have at the least an unpaired electron.
Write the chemical equation for reaction
that is
2SO2+O2 --->2SO2
find the moles of SO2 used = moles=mass/molar mass of so2
= 32g/80g/mol=0.4 moles
by use of reacting ratio between SO2 and SO3 which is 2:2 therefore the moles of so3 is also = 0.4 moles
STP 1 mole = 22.4L.
what about 0.4moles
= 0.4 /1 x22.4=8.96 liters
Answer:
Explanation:
You would have to add up the atomic masses of all the compounds in the compound, making sure you include how many molecules of each are in the compound
For example, in CuSOA we have 1 molecule of Cu and S, as 4 molecules of O
The atomic masses are as follows:
Cu = 63.55 u
S = 32.065 u
O = 15.99 units
This is how we would add it up:
(Atomic mass of Cu) + (Atomic mass of S) + 4(Atomic Mass of O)
(63.55) + (32.065) + 4(15.99)
(63.55) + (32.065) + 63.96
= 159.575 u
Answer:
a. Cyclohexanone
Explanation:
The principle of IR technique is based on the <u>vibration of the bonds</u> by using the energy that is in this region of the electromagnetic spectrum. For each bond, there is <em>a specific energy that generates a specific vibration</em>. In this case, you want to study the vibration that is given in the carbonyl group C=O. Which is located around 1700 cm-1.
Now, we must remember that the <u>lower the wavenumber we will have less energy</u>. So, what we should look for in these molecules, is a carbonyl group in which less energy is needed to vibrate since we look for the molecule with a smaller wavenumber.
If we look at the structure of all the molecules we will find that in the last three we have <u>heteroatoms</u> (atoms different to carbon I hydrogen) on the right side of the carbonyl group. These atoms allow the production of <u>resonance structures</u> which makes the molecule more stable. If the molecule is more stable we will need more energy to make it vibrate and therefore greater wavenumbers.
The molecule that fulfills this condition is the <u>cyclohexanone.</u>
See figure 1
I hope it helps!
Depending if the reaction is a reversible or an irreversible one, the direction of the arrow will point in one direction or 2 directions from reactants to products.