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- What is the relationship between this molecule and the others?Of two possible structures A and B for the conjugate acid of guanidine, the more stable is the one that is better stabilized by electron delocalization. Which one is it? Write resonance structures showing this electron delocalization.I ONLY NEED THE ANSWERS OF QUESTIONS 4, 5 and 6!! Explain briefly and clearly the following concepts, taking as reference the molecule of n-butane and the corresponding drawings or illustrations. See pages 149-152 of the book Organic Chemistry, sixth edition (J. G. Smith). 1. Potential energy of a conformation. 2. Dihedral angle (in chemical terms, nothing to do with planes) in relation to a rotatable bond for the molecule of interest. Present an example to illustrate the concept 3. What are the van der Waals interaction forces in a conformation? Then provide an illustration: 4. What is steric hindrance in a conformation? Then draw a picture to illustrate the concept? 5. What is the torsional stress of a conformation? Then draw a picture to illustrate the concept? 6. Describe 1,3-diaxial interaction and illustrate with a specific example.
- I know that the answer to this question is 60, but I am struggling to understand why. Could somebody please draw this out for me 3-dimensionally or explain to me in detail why this is the case? One explanation I've heard is that it is because when the dihedral angle between the two methyl groups is 60, the molecular dipole moment between the two chlorine atoms is the smallest, therefore the answer is 60. This explanation is meaningless to me - that does not even seem to be what the question is asking. Is it a poorly-worded question? i need good explanationGive a clear explanation handwritten in detailed of both subparts please2. What can you infer about the nature of the substituents? Provide at least two inferences and explain your basis using reliable sources.
- Can someone provide a step-by-step answer for the following blanks in the second table? Thank you in advance! :)If one molecule of HCl was to react with one molecule of caffeine, which N would be protonated? To answer this question, you will need to consider both the structure and the hybridization of the atoms. Justify your reasoningQuestion: What is the impact of molecular chirality on the pharmacological activity of drugs, and how can it be harnessed for the development of more effective therapeutic agents?