No they can not be identified through a karyotype such as sickle cell anemia cant be detected through karyotyping because there will be n observal change.
Hope this helps
Firstly the limiting reactant should be identified. Limiting reactant is the reactant that is in limited supply, the amount of product formed depends on the moles present of the limiting reactant.
the stoichiometry of x to y = 1:2
1 mole of x reacts with 2 moles of y
if x is the limiting reactant, there are 3 moles of x, then 6 moles of y should react, however there are only 4 moles of y. Therefore y is the limiting reactant and x is in excess.
4 moles of y reacts with 2 moles of x
since there are 3 moles of x initially and only 2 moles are used up, excess amount of x is 1 mol thats in excess.
Answer:
Since different isotopes of an element have different numbers of neutrons (but always the same number of protons) they have different mass numbers. Nitrogen-14 and nitrogen-15 are both stable isotopes of nitrogen. However, the other 5 isotopes are all unstable.
<u>Given:</u>
Initial amount of carbon, A₀ = 16 g
Decay model = 16exp(-0.000121t)
t = 90769076 years
<u>To determine:</u>
the amount of C-14 after 90769076 years
<u>Explanation:</u>
The radioactive decay model can be expressed as:
A = A₀exp(-kt)
where A = concentration of the radioactive species after time t
A₀ = initial concentration
k = decay constant
Based on the given data :
A = 16 * exp(-0.000121*90769076) = 16(0) = 0
Ans: Based on the decay model there will be no C-14 left after 90769076 years
Answer:
cannot be broken down further
