The compounds in each part below have the same (or similar) molecular weights. Which compound in cach part would you expect to have the higher boiling point? Explain your answers. (a) OH or (c) он HO HO. (b) (CH),N or N.
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- Using the degrees of unsaturation, determine the molecular formula for the following compound (NOT use subscripts )3. Arrange the following four compounds in order of increasing boiling point, and briefly explain your answers: 2-methylhexane, 1-heptanol, heptane, 3,3-dimethylpentane:Complete the following noting structures for A, B, and C. If more than one step is required to list them as 1, 2, 3, and so on.
- Compound D and compound E are in equilibrium. Write a stepwise mechanism from compound D to compound E showing ALL intermediates. Use curved arrows to symbolize the flow of electrons to show how each of the intermediates and product are formed. Show necessary lone pairs and all formal charges. Lastly explain which compound (D or E) will be in higher concentration.2. What can you infer about the nature of the substituents? Provide at least two inferences and explain your basis using reliable sources.Using the information provided below, deduce the identity of the compound I, II, III, IV and V. What is the IUPAC name of compound I, II, III, IV and V?
- Compound A and compound B are in equilibrium. Write a stepwise mechanism from compound Ato compound B showing ALL intermediates. Use curved arrows to symbolize the flow of electrons to show how each of the intermediates and products are formed. Show all lone pairs and formal charges. Lastly, explain which compound (Aor B) will be in higher concentration.Two constitutional isomers with molecular formula C2H6O have boiling points of –23.6°C and 78.4°C. Draw both constitutional isomers of C2H6O (or provide the name). Identify the structural class of each. Match the constitutional isomers you have drawn to the boiling points provided above, and explain your reasoning.Give a clear handwritten answer with explanation needed of each compound !!!
- Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Identification of Functional GroupsFunctional Groups of Classes of Organic Compounds.*Encircle the functional groups**For phenols and aryl halides, include the aromatic ring. For alcohols and alkyl halides, just encircle the –OH of –X group.how many degree of unsaturation are there in caffeine, C8H10N4O2? (Please show how do you know) A. 2 B. 4 C. 5 D. 6In the space provided below, write a line structure corresponding to the systematic name (R)-3-methylhexane. Then, provide a Newman projection that illustrates the highest energy conformation of (R)-3-methylhexane along the C3-C4 bond axis of the same. Again, place your answer in the space provided.