Answer: Option (d) is the correct answer.
Explanation:
It is given that molecular formula is 
. Now, we will calculate the degree of unsaturation as follows.
Degree of unsaturation = 
= 
= 9 - 8 + 1
= 2
As the degree of unsaturation comes out to be 2. It means that this compound will contain one ring and one double bond.
Yes, this compound could be an alkyne as for alkyne D.B.E = 2.
But this compound cannot be a cycloalkane because for a cycloalkane D.B.E = 1 which is due to the ring only.
Thus, we can conclude that it is a cycloalkane is not a structural possibility for this hydrocarbon.
I want to say addition. But I have a tendency to be wrong
Answer: 4.21×10⁻⁸
Explanation:
1) Assume a general equation for the ionization of the weak acid:
Let HA be the weak acid, then the ionization equation is:
HA ⇄ H⁺ + A⁻
2) Then, the expression for the ionization constant is:
Ka = [H⁺][A⁻] / [HA]
There, [H⁺] = [A⁻], and [HA] = 0.150 M (data given)
3) So, you need to determine [H⁺] which you do from the pH.
By definition, pH = - log [H⁺]
And from the data given pH = 4.1
⇒ 4.10 = - log [H⁺] ⇒ [H⁺] = antilog (- 4.10) = 7.94×10⁻⁵
4) Now you have all the values to calculate the expression for Ka:
ka = 7.94×10⁻⁵ × 7.94×10⁻⁵ / 0.150 = 4.21×10⁻⁸
Answer:
Lithium
Explanation:
I believe it is Lithium. It can easily be cut with a knife and is the 3rd lightest non gas on the periodic table that is not a gas.
Answer:
The correct answer is: <em>They each partially describe the bonding in a molecule.</em>
Explanation:
Some chemical molecules cannot be described completely by using only one Lewis structure. In these cases, we can describe the molecule by drawing 2 or more Lewis structures, and the structures are called <u>resonance structures</u>. The overall molecular structure is explained by all the resonance structures together. So, they each describe the bonding in the molecule only partially.
