Answer:
(C5H7)8
Explanation:
It's empirical formula is given as; C5H7
Molar mass of carbon(C) = 12 g/mol
Molar mass of hydrogen(H) = 1 g/mol
We are told that it's molar mass is 536 g/mol.
To find the molecular formula;
Molecular formula = n × empirical formula
Thus;
n = 536/((12 × 5) + (1 × 7))
n = 8
Thus;
Molecular formula = (C5H7)8
Answer:
oil = burn for 8 days = absurd = doesnt make sense but it happened lol
Explanation:
The reducing agent can approach the carbonyl face of camphor by forming a one carbon bridge (known as an exo attack) or a two carbon bridge (termed endo).
The two resultant stereoisomers are known as isoborneol and borneol (from exo attack) (from endo attack). Gas chromatography (GC) analysis may be used to calculate the ratio of each isomeric alcohol in the mixture. Unfortunately, IR analysis does not permit this.
The stereochemistry of the reaction is regulated in stiff cyclic compounds like camphor and norcamphor by protecting one side of the carbonyl group from the reagent's assault. The hydrogen atom is added to the endo side, creating the exo alcohol isoborneol, while the methyl groups on the one-carbon bridge of camphor screen the approach of the hydride from the "top" or exo side of the two-carbon bridge. You will be asked to guess the main isomeric alcohol created by the norcamphor hydride reduction later in the lab report.
To view more about rational reaction, refer to:
brainly.com/question/20308523
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