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5. The elimination reaction below produces 5 isomeric alkene products. Draw these 5 structures and give...
6. When the alkene shown below is treated with NBS, two isomeric products (ignoring R/S stereoisomers) are formed. A. (4 points) Draw the structures of these two products. (Hint: do part "B" first) NBS hv/CCl4 (4 points) Draw the structure of the allylic radical that is formed at the beginning of the propagation step, and then draw its resonance structure. B. C. (4 points) Draw the structure of the MAIOR product and give reasons for your choice.
draw the structure and the IUPAC names of the alkene products that would form in the acid catalyzed dehydration of 2,3-dimethyl-3-pentanol give them step mechanism for the formation of each product?,
for (1d.) Give the IUPAC name for the following structures including the configuration of the alkene. _______________ e. 4-propylhex-3-enamine for (1e.) Draw the structures for the guven iupac name. но d.
d Both elimination reaction. Experimental evidence shows that this reaction produces the less-substituted alkene as the sole product, as shown. Draw a reaction mechanism and give a rational explanation for this observation and discuss why the more-substi formed. (10 points) The fe he OCH,CH3 CH,CH2OH CH2CHs CH2CH3 OTs
1. The reaction below produces two products that are isomers of some kind. Draw both products and state their isomeric relationship. HBr 2. Provide a mechanism for the reaction below. a D 2 you wote, moyo OH H2SO4 HO
5. The reaction below produces TWO different products from an E2 reaction pathway. Identify both elimination products from this reaction. HINT: One of the elimination products should be relative easy to identify; the other elimination product is more challenging to determine. As a starting point, identify the most acidic proton in the substrate. NaoMe
5. The reaction below produces TWO different products from an E2 reaction pathway. Identify both elimination products from this reaction. HINT: One of the elimination products should be relative easy to identify; the other elimination product is more challenging to determine. As a starting point, identify the most acidic proton in the substrate. Nao Me
5. (4 pts) From the alkene, generate the two possible isomeric carbocations. Then draw the major (Markovnikov) product and the minor (anti-Markovnikov) addition products. No mechanism needed. HBr
3) Predict the major thermodynamic product for the elimination reaction below. OH 4) Draw a type of base that would give a different alkene product in the reaction in problem #3? As in more substituted vs. less substituted products.
Draw ALL possible unimolecular elimination (E1) products formed under the reaction conditions below; don't worry about specifving the maior vs, minor products. Where relevant, indicate the stereochemical outcome. 1. OTf E1OH 70 °C