6. Analysis of racemic fluoxetine hydrochloride by mass spectrometry gave, unsurprisingly, a main peak of exactly the same m/z value as that observed for either enantiomer in pure form. The mass spectrum of (S)-fluoxetine oxalate also showed the same main m/z peak. Explain these observations. [The molecular formulae of (R)- and (S)-fluoxetine hydrochloride is C17H19CIF3NO; the molecular formula of (S)-fluoxetine oxalate is C19H20F3O5.]

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Chapter12: Structure Determination: Mass Spectrometry And Infrared Spectroscopy
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6.
7.
Analysis of racemic fluoxetine hydrochloride by mass spectrometry gave,
unsurprisingly, a main peak of exactly the same m/z value as that observed for
either enantiomer in pure form. The mass spectrum of (S)-fluoxetine oxalate
also showed the same main m/z peak. Explain these observations.
[The molecular formulae of (R)- and (S)-fluoxetine hydrochloride is
C17H19CIF3NO; the molecular formula of (S)-fluoxetine oxalate is C19H20F3O5.]
How many sp-hybridised, sp²-hybridised and sp³-hybridised carbon atoms are
present in the structur of acyl chloride 4?
F3C
Transcribed Image Text:6. 7. Analysis of racemic fluoxetine hydrochloride by mass spectrometry gave, unsurprisingly, a main peak of exactly the same m/z value as that observed for either enantiomer in pure form. The mass spectrum of (S)-fluoxetine oxalate also showed the same main m/z peak. Explain these observations. [The molecular formulae of (R)- and (S)-fluoxetine hydrochloride is C17H19CIF3NO; the molecular formula of (S)-fluoxetine oxalate is C19H20F3O5.] How many sp-hybridised, sp²-hybridised and sp³-hybridised carbon atoms are present in the structur of acyl chloride 4? F3C
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