It should be B. All of the other choices are used often by abusers
Answer:
13 km
Explanation:
Distance travelled = 5 km + 3 km + 2 km + 3 km = 13 km
Answer:
For part (a): pHsol=2.22
Explanation:
I will show you how to solve part (a), so that you can use this example to solve part (b) on your own.
So, you're dealing with formic acid, HCOOH, a weak acid that does not dissociate completely in aqueous solution. This means that an equilibrium will be established between the unionized and ionized forms of the acid.
You can use an ICE table and the initial concentration ofthe acid to determine the concentrations of the conjugate base and of the hydronium ions tha are produced when the acid ionizes
HCOOH(aq]+H2O(l]⇌ HCOO−(aq] + H3O+(aq]
I 0.20 0 0
C (−x) (+x) (+x)
E (0.20−x) x x
You need to use the acid's pKa to determine its acid dissociation constant, Ka, which is equal to
Answer:
The atoms in the first period have electrons in 1 energy level. The atoms in the second period have electrons in 2 energy levels. The atoms in the third period have electrons in 3 energy levels. The atoms in the fourth period have electrons in 4 energy levels.
Answer:
- <u><em>butylphenyl ether.</em></u>
Explanation:
The formula of the compound is:
- CH₃ - CH₂ - CH₂ - CH₂ - O - C₆H₅
1. The functional group is of the kind R - O - R', i.e. two alkyl groups each attached to one end of the oxygen atom. That means that the compound is an ether.
2. One group attached to the oxygen group is CH₃ - CH₂ - CH₂ - CH₂ - which has 4 carbons and is named butyl group.
3. The other group attached to the oxygen atom is C₆H₅ - which is derived from ciclohexane as is known as phenyl group.
4. Using the rule of naming the subtituents in alphabetical order, you name butyl first and phenyl second, so it is <u><em>butylphenyl ether.</em></u>
