A.) CIS/Trans isomers
b.) constitutional isomers
c.) identical
d.) constitutional isomers
e.) identical
374u
187u
C₁₄H₂₂N₄O₈
Explanation:
To find the molecular weight of the compound C₁₄H₂₂N₄O₈ we simply sum that atomic masses of the given elements in the compound.
The empirical weight is determined by using the simplest ratio of the elements involved in the compound;
Molecular weight of C₁₄H₂₂N₄O₈;
atomic mass of C = 12g/mol
H = 1g/mol
N = 14g/mol
O = 16g/mol
Molecular weight = 14(12) + 22(1) + 4(14) + 8(16)
= 168 + 22 + 56 + 128
= 374u
Empirical weight:
Empirical formula:
C₁₄ H₂₂ N₄ O₈
14 : 22 : 4 : 8
divide by 2:
7 : 11 : 2 : 4
empirical formula C₇H₁₁N₂O₄
empirical weight =
=
= 187u
The molecular formula is the actual combination of atoms in a compound. so the molecular formula of the compound is C₁₄H₂₂N₄O₈
learn more:
Molecular mass brainly.com/question/5546238
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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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Answer choice "A. Defrostration " is the only "natural" cause of soil erosion
Answer:
Meerkats can be found in the desert.