1. What are possible alkyl halides formed for radical chlorination of ethane? Draw all the structures. 2. Give the possible product(s) (may be more than one product in each step) for A, B, and C in the following reactions. Mg H20 в NBS A hv/heat dry ether
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- What alkane is needed to make each alkyl halide by radical halogenation?Consider the following alkyl halides: - may react with NaI to give JKL? - an alkyl iodide that will give SN1 and E1 product? - has the highest boiling point? - most likely to give retention and inversion products in SN1 reaction? - most likely to give rearrangement product in SN1?Resveratrol is an antioxidant found in the skin of red grapes. Its anticancer, anti-inammatory, and various cardiovascular effects are under active investigation. (a) Draw all resonance structures for the radical that results from homolysis of the OH bond shown in red. (b) Explain why homolysis of this OH bond is preferred to homolysis of either OH bond in the other benzene ring.
- What alkane is needed to make each attached alkyl halide by radicalhalogenation?About: Substitution vs. Elimination Reactions Note: Identify the major and minor product (s) that are expected for each of the following reactions.If reacted with Cl2 how many distinct mini chlorinated products will be present? How many monocholtinated products will form at 1 and 2? Which Carbon will be attached to a Cl in the major product?
- Indane can undergo free-radical chlorination at any of the alkyl positions onthe aliphatic ring.Draw the possible dichlorinated products from this reaction.For SN2 Explain the order in which 1o (primary) alkyl halides reacted and explain why. The 1o primary alkyl halides are: (see picture below) 1-chlorobutane 1-bromobutane 1-chloro-2butene benzylchloridedraw the potential products in the space below, for the halogenation (with heat/UW light) reaction:
- reaction by filling in any Starting materials, reagents or products as needed.Draw the products of radical chlorination and bromination of eachcompound. For which compounds is a single constitutional isomerformed for both reactions? What must be true about the structure of areactant for both reactions to form a single product ?Does dehydrogenation of alkyl halides create Zaitsef or Hoffman products? In this example, which is created? I think it's Hoffman because there is a more stable/substituted option which is to put the double bond to the right of the positive charge instead of to the left. Or does it depend on the reactants? Further clarification is needed. Thank you in advance!