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- Which of the following choices is a diastereomer of the first structure shown? II IV O II O IVBr Br g. h. Br Br Br i. CI m. in. OH Он 2b. Which of the above compounds are optically active? 2c. Which of the above compounds are meso?Given the following compounds and boiling points: Determine the IMFs Order the compounds from weakest to strongest IMFs, and Pentane (C5H12) 36°C Methane (CH4) -164°C Sodium n-butoxide (C4H9NaO) +260°C Hydrogen dioxide (H2O) 100°C
- s 2req 2req 2req 2req 2req Visited Complete the equation for the following reaction by drawing a structural formula for the missing organic product. Onomorecom NH3 CH₂ + You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. • Draw cations and anions in separate sketchers. Ⓒ%81 CH₂ H₂O ? Y Jn [1Calculate the bio-degradation index for chlorobenzene (C6H5C1). HC HC cl CH CH CH2. With as much specificity as possible, how would each of the following molecules be classified? NR RO NR₂ R NG:S R₂N NR₂
- Which statement is incorrect for the following compounds? CH3 H H. ČH3 ČH3 H CH3 CH3 H I II III I and Il are diasteroisomers III is the meso compound I and II are enantiomers I and III are diasteroisomershow many of the compounds below are chiralConsider the stereochemistry of the equimolar mixture of compounds and its optical activity. Flm H3C F Which statement is true? Select one: the mixture is optically active the optical activity of the mixture cannot be determined by the information presented the mixture is optically inactive