Please correct answer and don't used hand raiting Designate the configuration of the stereogenic centre in the followingstructure according to the (R,S)-system and explain your answer.HOF-EtH

To designate the configuration of the stereogenic center in 1-fluoropropan-1-ol according to the…

Answered: Designate the configuration of the…

Organic Chemistry

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Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

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Problem 25VC: The following molecular model of a dimethyl-substituted biphenyl represents the lowest-energy...

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An acid–base reaction of (R)-sec-butylamine with a racemic mixture of 2-phenylpropanoic acid forms two products having different melting pointsand somewhat different solubilities. Draw the structure of these twoproducts. Assign R and S to any stereogenic centers in the products.How are the two products related? Choose from enantiomers,diastereomers, constitutional isomers, or not isomers of each other.
Is amitriptyline chiral? If so, how many of the possible stereoisomers are formed in this synthesis?
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Which of the following distinguished scientists is correctly identified? There may be more than one correct answer. Adolf von Baeyer proposed the importance of ring strain Louis Vuitton separated crystals of tartaric acid and hence isolated enantiomers of tartaric acid Vladimir Prelog worked with Robert S. Cahn and Sir Christopher Ingold to establish the Cahn-Ingold-Prelog priority system for nomenclature Emil Fischer invented the Fischer projection to facilitate the depiction of stereochemical relationships.
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7.(a) Draw and label (i) the enantiomer and (ii) a pair of diasteromers of the following compound. OH (b) Will a 50:50 mix of the enantiomers that you drew for 7al be optically active (rotate plane polarized light). Explain the reason for your answer b) Will a 50:50 mix of the two diasteriomers_you drew for 7bii be optically active (rotate plane polarized light). Explain the reason for your answer
Consider the substitution reaction that takes place when (S)-3-bromo-2,3-dimethylhexane is treated with ethanol. Which of the following would be true? The reaction would take place only with inversion of configuration at the stereogenic centre. The reaction would take place only with retention of configuration at the stereogenic centre. The reaction would take place with racemisation. No reaction would take place.
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Designate the configuration of the stereogenic centre in the following structure according to the (R,S)-system and explain your answer. HO F-Et H