An acid-base reaction or a neutralization reaction is a <u>chemical reaction that occurs between an acid and a base producing a salt and water</u>. The acids and bases can be strong or weak depending on their degree of ionization in water.
Butyric acid is a weak acid and in water it is ionized in the following way, loosing a proton (H+):
HC4H7O2 (aq) ⇆ H+ (aq) + C4H7O2- (aq)
On the other hand, potassium hydroxide is a strong base, so it will be completely ionized in water:
KOH(aq) → K+(aq) + OH-(aq)
Then the <u>net acid-base reaction</u> between butyric acid and KOH is:
HC4H7O2 (aq) + OH- (aq) ⇆ H2O + C4H7O2- (aq)
It is valid to consider only the OH- produced from the ionization of KOH in water since, as mentioned, this molecule is completely ionized. Also, we do not include the K + in the net equation since it is a spectator ion, it does not undergo chemical changes.
hooc are carboxyl groups
your r or amino groups are those unique structures which have different atoms in them. your nh2 groups are your hydrogen atoms
To find the mole of a substance, you take the mass divided by the molar mass of that substance~
Answer:
B) Electrons are located in the cloud-like areas around the nucleus.
Explanation:
The quantum mechanical model of the atom does not consider the path through which an electron travels. It rather estimates the probability of where electrons can be found at each energy level.
The region of maximum probability of where an electron is located is sometimes called an electron cloud or orbital. Each orbital of an atom and the electrons accomodated are described completely by a set of four quantum numbers.
Answer:
- Elimination
- Elimination
- Zaitsev
- Zaitsev
- Carbocation
Explanation:
- The mechanism is generally accepted to always operate via an ELIMINATION step-wise process.
- The ELIMINATION mechanism process will always produce (after dehydration) a ZAITSEV style alkene as major product
- The driving force for the production of this ZAITSEV style alkene product is generally going to be determined by stability of the CARBOCATION
Elimination mechanism is the removal of two substituents from a molecule in either a one- or two-step mechanism
Carbocation is a molecule containing a positive charged carbon atom and three bonds