Select the correct IUPAC name for the following organic substrate, including the R or S designation where appropriate, and draw the major organic product(s) for the SN 1 reaction. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Br H₂O Select Draw Templates More CH 0 Erase
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- A hydrocarbon of unknown structure has the formula C8H10. On catalytic hydrogenation over the Lindlar catalyst, 1 equivalent of Η2 is absorbed. On hydrogenation overa palladium catalyst, 3 equivalents of Η2 are absorbed. (a) How many degrees of unsaturation are present in the unknown structure? (b) How many triple bonds are Present? (c) How many double bonds are present? (d) How many rings are present? (e) Draw a structure that fits the data.Please answer ASAP Draw the arrow-pushing mechanism for the following reaction. 1) P(OCH2CH3)3, NaH 2) 4-Methyl-2-PentanoneQa 18. Bromination of 5a-cholestan-3-one occurs at C-2 or C-4 to give 2 regioisomers. Two unsaturated ketones with lambdamax = 230 nm and lambdamax = 241 nm are yielded during dehydrobromination. Use Woodward-Fieser rules to distinguish between the two.
- For the following question please: 1. Predict the products: 2. Give the correct mechanism via correct arrow pushing, and arrow formalisms: 3. Name each mechanism 4. Name each MAJOR and MINOR products: (S)-2-iodobutane + KOH/DMFWhy are SN1 reactions favored by polar protic solvents? Group of answer choices Polar protic solvents stabilize reaction intermediates Polar protic solvents cannot form hydrogen bonds. Polar protic solvents contribute leaving groups. Polar protic solvents contribute leaving groups.Give the organic product formed in each of the following reactions, draw a 3-D representation for the product molecule showing the correct configuration
- Which reagent is required to complete the reaction in Figure 11? [Generate a SMILES notation: https://jsme-editor.github.io/dist/JSME_test.html. Copy the notation (CTRL+C) and paste it as the answer to this question (CTRL+V).] * Your answerDraw the structure of the major and minor organic product(s); provide the reactants, or provide the starting material for each of the following reactions. Indicate which products) are major and minor making sure to include stereochemistry when appropriate. If no reaction is predicted indicate such with "No Rxn"redraw the following reaction mechanism with benzene instead of isoborneol. it's an oxidation mechanism from OH to ketone. please include the arrow pushing.
- 2-butanol + NOx + hv (assume the carbon-hydrogen bond on the carbon adjacent to the carbonwith the alcohol group is the weakest) For each mechanism, provide the photolytic cycle, a source for hydroxyl radical (if needed) AND atermination step. You may stop when you have accounted for all radicals AND all VOCs are stable (i.e., ifformaldehyde is a product of your mechanism, you do not have to oxidize that molecule to).Draw the major product of this reaction. Ignore inorganic byproducts. 1. LiAIH4 2. Neutralizing work-upMatch the drugs with the corresponding Phase 1 reaction that will happen appropriately with the highligthed portion of the drug. A: C4 of Benzene ring B: Methyl group of Nitrogen C: -NH-NH2 moiety D: N,N-dimethyl moiety E: Ring S CHOICES: A. Desulfuration B. Aromatic hydroxylation C. Hydrazo reduction D. Nitro reduction E. Sulfur oxidation F. Deamination G. N-demethylation