The chemical compound's empirical formula is NS.
The chemical compound's molecular formula is N4S4.
<h3>What does a chemical empirical formula look like?</h3>
- The empirical formula of a compound that gives the proportion (ratios) of the elements in the complex but not the precise number or arrangement of atoms is known as an empirical formula.
- This would be the compound's element to whole number ratio with the lowest value.
<h3>What sort of empirical formula would that be?</h3>
- The chemical structure of glucose is C6H12O6. Every mole of carbon and oxygen is accompanied by two moles of hydrogen.
- Glucose has the empirical formula CH2O.
- Ribose has the chemical formula C5H10O5, which can be simplified to the empirical formula CH2O.
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the question you are looking for is
A compound containing only sulfur and nitrogen is 69.6% S by mass; the molar mass is 184 g/mol. What are the empirical and molecular formulas of the compound?
8
It’s 8 bc I said it was 8 ;)
Ribosomes hope this helps if not oh well
Answer:The product formed on reaction with hydroxide ion as nucleophile is 2R-hexane-2-ol.
The product formed on reaction with water would be a 50:50 mixture of
2S-hexane-2-ol. and 2R-hexane-2-ol.
Explanation:
2S-iodohexane on reactiong with hydroxide ion would undergo SN² substitution reaction that is substitution bimolecular. Hydroxide ion has a negative charge and hence it is a quite good nucleophile .
The rate of a SN² reaction depends on both the substrate and nucleophile . Here the substrate is a secondary carbon center having Iodine as a leaving group.SN² reaction takes place here as hydroxide ion is a good nucleophile and it can attack the secondary carbon center from the back side leading to the formation of 2R-hexane-2-ol.
In a SN² reaction since the the nucleophile attacks from the back-side so the product formation takes place with the inversion of configuration.
When the same substrate S-2-iodohexane undergoes a substitution reaction with water as a nucleophile then the reaction occurs through (SN¹) substitution nucleophilic unimolecular mechanism .
The rate of a SN¹ reaction depends only on the nature of substrate and is independent of the nature of nucleophile.
The SN¹ reaction is a 2 step reaction , in the first step leaving group leaves leading to the formation of a carbocation and once the carbocation is formed then any weaker nucleophile or even solvent molecules can attack leading the formation of products.
In this case a secondary carbocation would be generated in the first step and then water will attack this carbocation to form the product in the second step.
The product formed on using water as a nucleophile would be a racemic mixture of R and S isomers of hexane -2-ol in 50:50 ratio. The two products formed would be 2R-hexane-2-ol and 2S-hexane-2-ol.
Kindly refer the attachment for reaction mechanism and structure of products.
60 g C2H6 × 1 mol C2H6 x 7 mol O2 x 32 g O2 = ~223.5 g O2
30.068 g 2 mol C2H6 1 mol O2