Answer:
Yellow seeds
Explanation:
Dominant traits are those that are inherited unchanged in a hybridization like the yellow seeds.
We call these reactive elements, becausethese atoms really like to follow the buddysystem and form bonds with other atoms.Noble gases, however, don't have thisproblem. Their outer shells are filled to the max, so they don't need to bond or react with any other atoms.
Answer:
<u>(A) Plants would probably not have enough nitrogen.</u>
Explanation:
<em>According to the passage, bacteria help us digest our food and make yogurt. But it is the bacteria in the soil specifically that "Cycle nitrogen through the ecosystem, which plants rely on"</em>
Fluorine is the most active chemical element, reacting with virtually every element. It even reacts with the noble gases at high temperatures and pressures. The noble gases, or Group 18 (VIIIA), also known as the inert gases, generally do not react with other elements.
Explanation:
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!