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Consider the following hydrocarbons:
I. butane II. methyl benzene III. octane IV. benzene
Which of the following will produce a less soothy upon ignition?
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- Organic Chemistry Explain your answer clearly and in a step-by-step fashion. Do not leave any details out. Describe everything in detail and do not skip steps and explain as much as you can.Explain the role strain plays on stability and reactivity of a cyclic alkane such as cyclopropane.The skeletal line formula for a branched alkene is shown below. (i) What is the molecular formula of this compound? (ii) How many carbon atoms are in the longest chain, ignoring the double bond? (iii) What is the longest chain incorporating both carbons of the double bond? (iv) How many substituents are on this chain? (v) Give the IUPAC name for this compound. [6]
- What functional group is at 763ppm? For HNMR at about 2.3ppm is it a quintuplet? How do I get the structure from this?Consider the following proposed structures for benzene, each of which is consistent with the molecular formula C6H6. (iv) CH3CCCCCH3 (v) CH2=CHCCH=CH2 When benzene reacts with chlorine to give C6H5Cl, only one isomer of that compound forms. Which of the five proposed structures for benzene are consistent with this observation? When C6H5Cl reacts further with chlorine to give C6H4Cl2, exactly three isomers of the latter compound form. Which of the five proposed structures for benzene are consistent with this observation?1. What is resonance theory? State five conclusionstgan can be drawn from the theory. 2.What factors confer aromaticity to an organic molecule. 3. What are the various ways by which alkenes can be synthesized. 4. State the two main experiment that were used to establish the extra stability of the benzene molecule.
- Organic Chemistry! I need help with writing the products of the reactions. I would appreciate it if it was in line structure form, Thank you.give the nomenclature or the structure of the following molecules of item #21 to #25.for part b）why do we write AlCl3 at top of the arrow and AlCl4 at the bottom of arrow？？is it any connection between the two？does it means that AlCl 4 need to be present in order to make AlCl3 reacts to the molecule and make the reaction to process？？ 2. why when AlCl3 added，Cl was removed from the ring？what princeiple theory is that ？ 2. when SO3 is added ，SO3 attached to the ring，why ？what principle is behind this phenamonane 3.Just confused about why AlCl3 removes Cl from the ring，while HSO3 donate SO3 to the ring. Is it Something about nucleohilic or eletrciohillic？