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- Assign the following alkene molecules as being cis or trans, E or Z isomers• Identify each of the following alkenes that can exist as a pair of diaste reomers. Write the structures of the pair of diastereomers in each case. 1. CH, СН-CHCH, 2. (CH,),C=CHCI 3. BRFC=CHCH, 4. F,C=CCl,Please draw the line structures for the C8H17+ carbocations that have the carbon skeleton below And please circle the most stable carbocation
- Explain the role strain plays on stability and reactivity of a cyclic alkane such as cyclopropane.Draw the Structure for the heterocyclic compound with the following systematic name: 2-Ethyl-4chloro-1,3-thiazineDraw the structures of two alkenes that would react to form the haloalkane below upon addition of HBr. Your alkenes should be different regioisomers that yield the haloalkane as the major product without requiring rearrangement to occur.
- Draw the line bond structures for the following alkenes, cyclic alkenes, and alkynes: Can you explain to me about this part A) noncyclic alkenes that contain 4 carbon atoms (3 possible), please? Can you explain to me about this part B) cyclic alkenes that contain 4 carbon atoms (4 possible), please? Can you explain to me about this part C) alkynes that contain 4 carbon atoms (2 possible, neither of them is a cyclic alkyne), please?Which of these alkenes show cis-trans isomerism? For each that does, draw structural formulas for both isomers.Using Zaitsev's rule, choose the most stable alkene among the following. Draw out the structures of each of the options then select the correct answer. Recall that Zaitsev's Rule is about alkene stability. The trend for this is similar to the trend for carbocation stability. Either more or fewer groups on the alkene (and the carbocation) make it more stable. This question is wanting you to remember if it's more or fewer. A) 1,2-dimethylcyclohexene B) 1,6-dimethylcyclohexene C) cis-3,4-dimethylcyclohexene D) They are all of equal stability according to Zaitsev's rule. Provide the major dehydration product of the following reaction. Recall which of the four substitution and elimination reactions a dehydration is. Before you do your S# or EF mechanism, remember what heteroatoms do in the presence of an acid (aka-the-OH is a bad leaving group, but protonating it might turn it into a good one). Don't forget to apply the concept from the previous question. OH Ht A
