The compound : C₄₀H₄₄N₄O
<h3>Further explanation</h3>
The empirical formula is the smallest comparison of atoms of compound =mole ratio of the components
The principle of determining empirical formula
• Determine the mass ratio of the constituent elements of the compound.
• Determine the mole ratio by dividing the percentage by the atomic mass
The mol ratio of composition : C : H : N : O

<span>The reason it will be 7 for some titrations is that when you titrates a strong acid with a strong base for example HCl and NaOH the salt formed is conjugate base of strong acid and will be a very weak base
That means that it cannot produce any OH^-1 and all the H+ has been converted to water.The only source of H+ or OH is water with a Ka of 10^-14 so the pH = -log [H+]=-log 10^-7 = 7
second reason is
When you titrates a weak acid with strong base at equivalence point
only a water solution of the conjugate base exists
CH3COOH + NaOH ----- Na+ CH3COO^-1 + H2O
Since the conjugate base is the conjugate base of a weak acid it will hydrolyze in water like so
for instance Na+ CH3COO^-1 + HCl---- CH3COOH + NaCl the equivalence point will be way BELOW 7 and in the case of above will be less than 5. So pH of 7 at equivalence point is only reached in strong acid strong base titrations.
hope this helps</span>
Given equation:
P + O2 → P2O5
In order for the equation to be balanced, the stoichiometry of the atoms of one kind on the reactant side must be equal to that on the product
Reactants Products
P = 1 P = 2
O = 2 O = 5
The balanced equation would be:
4P + 5O2 → 2P2O5
Reactants Products
P = 4 P = 4
O = 10 O = 10
Ans: D)
Answer:
The three-step synthesis of trans-2-pentene from acetylene is as follows.
<u>Step -1:</u> Formation of higher order terminal alkyne on reaction with sodium acetylides with haloalkanes.
<u>Step -2:</u> Formation terminal alkyne to nonterminal alkynes.
<u>Step -3:</u> Formation of trans-pent - 2-pent-ene by reduction.
Explanation:
Synthesis of trans-pent-2-yne from ethyne takes place is mainly a three step synthesis which involves formation of higher order terminal alkyne on reaction with sodium acetylides with haloalkane. Second step involves the further alkylation of terminal alkynes to higher order nonterminal alkynes and the third step involves the formation of trans-2-ene by dissolving reduction method.
The chemical reaction of each step of chemical reactions is as follows.