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Predicts the products or starting material of the following allende addition reactions. Put your answers (organic products only) in the indicated boxes.
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- 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 ACan you please tell me if I did these right and am understanding the concept of OsO4? I know it reacts with the most substituted alkene. ThanksTrue or False A nucleophile is any atom or molecule which can attack positively or partially positively charged molecules or atoms
- Claisen Condensations (Esters) 1. NaOEt EtO 2. H3O+ м Eto MechanismA benzene ring alters the reactivity of a neighboring group in the so-called “benzylic” position, similarly to how a double bond alters the reactivity of groups in the “allylic” position. Benzylic cations, anions, and radicals are all more stable than simple alkyl intermediates. a) Use resonance structures to show the delocalization of the positive charge, negative charge, and unpaired electron of the benzyl cation, anion, and radical.Determine whether the following reaction is an example of a nucleophilic substitution reaction: 8+ + H2O Molecule A Molecule B OH ++H Is this a nucleophilic substitution reaction? If this is a nucleophilic substitution reaction, answer the remaining questions in this table. What word or two-word phrase is used to describe the role Molecule A plays in this reaction? ☐ What word or two-word phrase is used to describe the role Molecule B plays in this reaction? What word or two-word phrase is used to describe the role of the carbon labeled with the 6+ symbol? What word or two-word phrase is used to describe the role of the atom or group highlighted in red? ☐ ☐ ☐ Yes No
- Draw out 3 molecules of CH3NH2 showing the strongest interactions that are present between the molecules.Which of the following is the electrophile in the sulfonation of benzene? Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. SO3+ b SO2+ H2SO4 d. SO3Determine the number of carbons present in the compound based on the base name. Draw the carbon chain and include any double or triple bonds if indicated in the suffix of the base name. Number each carbon. The carbons can be numbered from left to right or right to left. Draw any substituents on the corresponding carbon atom for which is indicated in the name. Refer to Figures 4 and 5 in the background for a visual representation of numbered carbons with corresponding substituents. Check that each carbon atom has a total of 4 bonds.
- Please answer all of it. If not, please skip. Draw the structure of a branched hydrocarbon that also contains at least one atom with trigonal planar geometry. Draw the structure of an aromatic hydrocarbon containing two halogens. Draw the structure of a molecule containing an aliphatic primary amine and a carboxyl group. Draw the structure of an acyclic molecule containing a primary and a secondary alcohol group. Draw the structure of an achiral tertiary alcoholOrganic Chemistry 1 Here is the professor's solution to the problem. However, I do NOT understand the solution. Please explain the answer in a clear step-by-step fashion to me. Explain the answer provided in the image in a clear fashion and as if I did not know much about organic chemistry. It seems to me like the professor is making the problem more complicated than it has to be. Can you demystify or simplify this problem about D glucose? How can you assign priorities on a Fischer projection? I don't get it. Here is the complete solution. Please explain it in a basic way.