b) 1. Ho, Lindlar 2. Br₂, DCM (CH₂C₁₂) Skeletal Structure The reaction above produces two enantiomers. Show the Perspective Formulas of each: 1
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- 5. (a) Identify the relationship of the two compounds below. (b) Write the most stable chair conformation for each. Br CH₂ and A. identical B. constitutional isomers C. stereoisomers D. unrelated Br CH₂(a)(2R,3S)-2,3-dibromohexane, draw a three-dimensional representation.1. (a) Provide a name for each molecule (I narrowed it down to three subparts)
- I need an explanation on this problem.3.) 2-Methylbutane (isopentane) is used, in conjunction with liquid nitrogen, to freeze tissues for cryosectioning in histology. Below is the potential energy diagram for all the conformers of 2-methylbutane. Provide structures that match structure A, B, and C in the boxes provided. B F IM C A potential energy Conformer A 0° D angle of internal rotation Conformer B E F H 360° (=0°) Conformer CUsing your model, construct an energy diagram to show the variation in the free energy of the molecule as the FRONT ATOM is rotated CLOCKWISE from 0º to 360º in 60º increments. In your energy diagram, you should clearly show the relative energies of each conformer.
- Q2. Which one of the following structures is the most stable conformation for 2-bromo butane (viewing down the C2-C3 bond axis where C2 is front carbon and C3 is back carbon) H H. H H. B ವಿಡಿಯ ಉನ್ದ ಮತ್ತೇರು ಮಟ್ಟದ CH₂ CH₂ CH₂ H (D) (A) (B)Show in each of the pairs below whether the two structures are structural isomers, stereoisomers, or different conformations of the same compound.2. Convert the following bond-line structure to Newman projections that represents it lowest energy and highest energy conformations. Look down the indicated C2-C3 bond. lowest energy highest energy
