Answer is: because carbon(IV) oxide is released.
For example if baking soda is used for <span>the pizza dough, than on heat carbon(IV) oxide is product of chemical reaction:
2NaHCO</span>₃ → Na₂CO₃ + CO₂ + H₂O.
If we use yeast (<span>single-celled microorganism)</span>, also carbon(IV) oxide produced, because yeast turns sugars into carbon(IV) oxide.
Answer:
Copper (I) hydroxide
Explanation:
Copper (I) hydroxide is a chemical compound with the chemical formula of CuOH. One copper atom (Cu), one oxygen atom (O), and one hydrogen atom (H.)
Explanation:
Conjugated diene is the one that contains alternate double bonds in its structure. That means both the double bonds are separated by a single bond.
Cumulated diene is the one that contains two double bonds on a single atom. This means it has two double bonds continuously.
Isolated double-bonded compound has a single bond isolated by two to three single bonds.
Compound A: Two alkenes are joined by a sigma bond.
For example:
It is a conjugated diene.
Compound B: Two alkenes are joined by a C H 2 group.
It is a cumulative diene.
Compound C: Two alkenes are joined by C H 2 C H 2.
Then it is an isolated alkene.
Compound D: A cyclohexene has a double bond between carbons 1 and 2. Carbon 3 is an sp 2 carbon that is bonded to another s p 2 carbon with an alkyl substituent.
Hence, compound D is a conjugated diene.
Answer:

Explanation:
To solve this problem, we can use the Combined Gas Laws:

Data:
p₁ = 1.7 kPa; V₁ = 7.5 m³; T₁ = -10 °C
p₂ = ?; V₂ = 3.8 m³; T₂ = 200 K
Calculations:
(a) Convert temperature to kelvins
T₁ = (-10 + 273.15) K = 263.15 K
(b) Calculate the pressure

Answer:
Product: ethyl L-valinate
Explanation:
If we want to understand what it is the molecule produced we have to an<u>alyze the reagents</u>. We have valine an <u>amino acid</u>, in this kind of compounds we have an <em>amine group</em> (
) and a <em>carboxylic acid</em> group (
). Additionally, we have an <u>alcohol </u>(
) in the presence of HCl (a <u>strong acid</u>) in the first step, and a base (
).
When we have an acid and an alcohol in a vessel we will have an <u>esterification reaction</u>. In other words, an ester is produced. As the <em>first step,</em> the oxygen in the C=O (in the carboxylic acid group) would be protonated. In the <em>second step</em>, the ethanol attacks the carbon in the C=O of the carboxylic acid group producing a new bond between the oxygen in the ethanol and the carbon in the carboxylic acid. In <em>step 3</em>, a proton is transferred to produce a better leaving group (
). In <em>step 4</em>, a water molecule leaves the main structure to produce again the double bond C=O. <em>Finally</em>, a base (
) removes the hydrogen from the C=O bond to produce ethyl L-valinate
See figure 1
I hope it helps!