Answer:
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Answer:
See explanation
Explanation:
The drug thalidomide with molecular formula C13H10N2O4 was widely prescribed by doctors for morning sickness in pregnant women in the 1960s.
The drug was sold as a racemic mixture (+)(R)-thalidomide and (-)(S)-thalidomide.
Unfortunately, only the (+)(R)-thalidomide exhibited the required effect while (-)(S)-thalidomide is a teratogen.
This goes a long way to underscore the importance of separation of enantiomers in drug production.
Therefore, all the teratogenic effects observed when using the drug thalidomide was actually as a result of the presence of (-)(S)-thalidomide, the unwanted enantiomer.
Hydrofluorocarbons (HFCs), perfluorocarbons (PFCs), sulfur hexafluoride (SF6) and nitrogen trifluoride (NF3).
<span>C4H4
The compound in question has an equal ratio of hydrogen and carbon. The atomic weight of carbon is roughly 12 and the atomic weight of hydrogen is roughly 1. The mass of the compound in question is roughly 52.
52/13=4
C4H4</span>