5. The correct name of the compound on the right is- B) (S)-2-bromobutane A) (R)-2-bromobutane C) (R)-2-bromopentane E) (S)-2-bromohexane D) (S)-2-bromopentane H Br H H CH3 CH2CH3
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- I posted this question afew times , but no one answered can you please help part D,E,F Can you please make sure the these answers are correct for part A,B ,C A) 1 chlorobutane 1 chlorobutane identical b) 2,3 dibromobutane 2,2 dibromotane isomers c) 2- methylpropane 2,2 dimthylpropane neitherc) For the IUPAC names below, provide an unambiguous structure! 1) (1R, 2R, 4S)-1,2-dibromo-4-methyl-cyclohexane 2) (2R, 3Z)-5-Fluoro-3-penten-1,2-diol5) Based on the structures of lycopene and ẞ-carotene, which are two chemicals found in another common vegetable, the tomato, answer the following questions: a) Are they stereoisomers, constitutional isomers or not even isomers? b) Do you expect them to be relatively polar or nonpolar substances? Why? c) How many double bonds are in lycopene? How many in ẞ-carotene? d) As lycopene is transformed into ẞ -carotene, how many pi electrons from the double bonds are transformed into single bonds? How many new single bonds are being formed in ẞ-carotene? e) The first step of a possible mechanism for the ring closure in the transformation is outlined below (only part of the structure is shown for simplicity). Draw the product that results from this arrow pushing mechanism. Be sure to include any formal charges that arise from the carbon atoms.
- Provide the correct systematic name for the compound shown here. ОН OIIII... CI 3-chloro cyclohexan-1-ol2. Which of the following compounds could have configurational isomerism (cis or trans) and if they do, draw the both of the structures and label them as cis and trans d) 1,2-dichloroethene e) 2-methyl-2-butene f) 1-chloropropeneDo you predict the product to be the cis isomer, the trans isomer, or a mixture of cis and trans isomers? Explain.
- Please answer my questionDraw the structure of the following compounds (E)-3,7-Dimethyloct-3-ene and NeopentylcyclohexaneFor the following, you must draw an appropriate structure that has the chemical formula C5H,NO with the indicated functional group(s) and/or property. In each case, identify any other functional groups in the molecule you draw, that were not indicated in the question. You may use condensed dash or bond-line structure to draw your molecules. a) An aldehyde b) A cyclic ether c) An acyclic amide that cannot form hydrogen bonds with itself