Answer:
58.9mL
Explanation:
Given parameters:
Initial volume = 34.3mL = 0.0343dm³
Initial concentration = 1.72mM = 1.72 x 10⁻³moldm⁻³
Final concentration = 1.00mM = 1 x 10⁻³ moldm⁻³
Unknown:
Final volume =?
Solution:
Often times, the concentration of a standard solution may have to be diluted to a lower one by adding distilled water. To find the find the final volume, we must recognize that the number of moles of the substance in initial and final solutions are the same.
Therefore;
C₁V₁ = C₂V₂
where C and V are concentration and 1 and 2 are initial and final states.
now input the variables;
1.72 x 10⁻³ x 0.0343 = 1 x 10⁻³ x V₂
V₂ = 0.0589dm³ = 58.9mL
Answer is: <span>excited state.
In </span>excited state, hydrogen has<span> higher </span>energy<span> than in the </span>ground state (state with lowest energy). H<span>ydrogen atom has one </span>electron<span> in the lowest possible </span>orbit<span> (1s), when atom absorbs</span><span> energy</span><span>, the electron move into an excited state (quantum numbers greater than the minimum possible). </span>Electron lifetime in excited state is short.
Transverse wave, motion in which all points on a wave oscillate along paths at right angles to the direction of the wave's advance. Surface ripples on water, seismic S (secondary) waves, and electromagnetic (e.g., radio and light) waves are examples of transverse waves.
Answer:
A true
Explanation:
Bald eagles have white heads distinguishing them from the rest of their body(which is dark brown
Answer:
see explanation below
Explanation:
You are missing the reaction scheme, but in picture 1, I found a question very similar to this, and after look into some other pages, I found the same scheme reaction, so I'm gonna work on this one, to show you how to solve it. Hopefully it will be the one you are asking.
According to the reaction scheme, in the first step we have NaNH2/NH3(l). This reactant is used to substract the most acidic hydrogen in the alkine there. In this case, it will substract the hydrogen from the carbon in the triple bond leaving something like this:
R: cyclopentane
R - C ≡ C (-)
Now, in the second step, this new product will experiment a SN2 reaction, and will attack to the CH3 - I forming another alkine as follow:
R - C ≡ C - CH3
Finally in the last step, Na in NH3 are reactants to promvove the hydrogenation of alkines. In this case, it will undergo hydrogenation in the triple bond and will form an alkene:
R - CH = CH - CH3
In picture 2, you have the reaction and mechanism.
