<h2>Answer:</h2>
It means the waves collides and constructive interference occurred.
<h3>Explanation:</h3>
If the two waves coming from the opposite direction collide with each other, there are two way of their interference.
- Constructive interference: An interference which results in the increase in energy. And it is when crust of a wave comes on the crust of second wave.
- Destructive interference: An interference which results in decrease in energy of the resulting wave and colliding waves cancel the result of each other.
Hence in experiment there will be constructive interference.
Answer:
NH3
Explanation:
2NH3(aq)+CO2(aq)→CH4N2O(aq)+H2O(l)
So for two moles of NH3 we need one mole of CO2. So let's count moles for each reagent.
n(NH3)=m(NH3)/M(NH3)=135700/17,03=7968.29 mol
n(CO2)=m(CO2)/M(CO2)=211400/44.01=4803.45 mol
From equation we have to divide n(NH3) by 2 because we need two equivalent per one CO2. That will be 3984.145. So the limiting agent is NH3 because it's not enough of it to react with all CO2
Cadium
Down a period, atomic radii decrease from left to right due to the increase in the number of protons and electrons across a period.
Answers:
1. 3-ethyl-3-methylheptane; 2. 2,2,3,3-tetramethylpentane; 3. hexa-2,4-diene.
Explanation:
<em>Structure 1
</em>
- Identify and name the longest continuous chain of carbon atoms (the main chain has 7 C; ∴ base name = heptane).
- Identify and name all the substituents [a 1C substituent (methyl) and a 2C substituent (methyl).
- Number the main chain from the end closest to a substituent.
- Identify the substituents by the number of the C atom on the main chain. Use hyphens between letters and numbers (3-methyl, 3-ethyl).
- Put the names of the substituents in alphabetical order in front of the base name with no spaces (3-ethyl-3-methylheptane)
<em>Structure 2</em>
- 5C. Base name = pentane
- Four methyl groups.
- Number from the left-hand end.
- If there is more than one substituent of the same type, identify each substituent by its locating number and use a multiplying prefix to show the number of each substituent. Use commas between numbers (2,2,3,3-tetramethyl).
- The name is 2,2,3,3-tetramethylpentane.
<em>Structure 3
</em>
- Identify and name the longest continuous chain of carbon atoms that passes through as many double bonds as possible. Drop the <em>-ne</em> ending of the alkane to get the root name <em>hexa-</em>.
- (No substituents).
- Number the main chain from the end closest to a double bond.
- If there is more than one double bond use a multiplying prefix to indicate the number of double bonds (two double bonds = diene) and use the smaller of the two numbers of the C=C atoms as the double bond locators (2,4-diene)
- Put the functional group name at the end of the root name (hexa-2,4-diene).
<em>Note</em>: The name 2,4-hexadiene is <em>acceptable</em>, but the <em>Preferred IUPAC Name</em> puts the locating numbers as close as possible in front of the groups they locate.