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Q: What is the product of this reaction? 1. LiAlH4 ??? не от 2.H+ ОН ada d Н н (В) (D) (A) ОН ОН ОН
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Q: NO2 HN H3C CH3 NO2
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Q: What is the major organic product of the following reaction
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Q: Draw the major product of this reaction. Ignore inorganic byproducts. NO2 1. LIAIH4 2. H3O*
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Q: 1) BH3, THF 2) H2O2 H,O, NAOH 10. 3) NaH 4) CH3B
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Q: Draw the major product of the reaction. OH NaH H2 NaBr + C6H100 DMF Br
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Q: Complete these SN2 reactions, showing the configuration of each product.
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Q: What is the product of this reaction? a) c) CH₂ MgCI CH3 CH3 1) CH₂MgCI 2) H₂O* b) d) LOH CH₂ LOH…
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Q: What is the major product to the following reaction? NaOCH3 OCH3 HOCH3 OCH3
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Q: Draw the major product of this reaction. Ignore inorganic byproducts and COM. 1. KMNO4, OH- (warm)…
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Q: What is the organic product obtained from the following reaction? CH,CO,H CH3 CH3 H3C H3C H3C CH H3C…
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Q: Br2 H20 CH2
A: Electrophilic addition of bromine to alkene Attack of water as nucleophile.
Q: 10. What is the major organic product obtained from the following reaction? b. 12 3 -CEN 1. NaOH,…
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Q: NaOCH; C H,OH heat CH3 H Br
A: This is an Elimination Reaction which takes place in presence of strong Base
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- Draw the organic product(s) of the following reaction. You do not have to consider stereochemistry. Include cationic counter-ions, e.g., Na+ in your answer, but draw them in their own sketcher. If no reaction occurs, draw the organic starting material. Separate multiple products using the + sign from the drop-down menu.Draw the structure(s) of the major organic product(s) obtained after workup of the following reaction. Use the wedge/hash bond tools to indicate stereochemistry where it exists. If no reaction occurs, draw the organic starting material. Draw structure(s) of product(s) after aqueous workup. Include counter-ions, e.g., Na+, I-, in your submission, but draw them in their own separate sketcher. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.True or False 1. Liebermann-Burchard Test -Color change is due to increasing conjugation of the double bond in adjacent fused ring 2. Liebermann-Burchard Test -Acetic anhydride reacts with the aliphatic hydrocarbon. 3. Salkowski Test - The chloroform layer turns red. 4. Salkowski Test - Involves the reagents chloroform, sulfuric acid and acetic anhydride 5. Liebermann-Burchard Test -Reaction involved is esterification. 6. Keller-Killiani Test - Involves color reaction of the sugar 2-deoxyhexose 7. Salkowski Test - The upper layer turns yellow with green fluorescence 8. Liebermann-Burchard Test -Must observe the color right away because it happens in a very short period of time. 9. Liebermann-Burchard Test - Chloroform was added to react with sulfuric acid. 10. Keller-Killiani Test - Color change results to reddish brown that turns into violet or purple
- Phineas and Ferbs, two brothers who enjoy vacations, doing fun things every summer. This summer the brothers and their friends carry out an organic synthesis with an unknown compound (L1) that contains 52% Carbon, 6% Hydrogen and 42% bromine, this compound (L1) is treated with magnesium in ether to obtain L2 , which reacts violently with D2O for 1-methyl cyclohexene with a deuterium atom in the methyl group (L3). The L2 reaction is treated with acetone followed by hydrolysis to give L4. Heating L4 with concentrated sulfuric acid gives L5, which decolors the bromine, obtaining L6. L5 undergoes hydrogenation with excess hydrogen and platinum as a catalyst giving rise to isobutyl cyclohexane. Determine the structures of compounds L1 through L6.Compound X is insoluble in cold KMnO4, Br2 in CCl4, and conc. H2SO4. Compound X is most likely: a. an alkane b. none of these c. an alkene d. an alcohol e. an alkyl halide Indicate which of the ff. statements regarding nucleophilicity is incorrect. F- is more nucleophilic, hence, more reactive towards methyl iodide than Cl-. Second row elements are more nucleophilic than first row elements of comparable basicity. The rate of SN2 reaction may be markedly affected by the nucleophilicity of the attacking atom. Nucleophilicity is the affinity of a nucleophile to an electrophilic carbon Which of the following alkynes can be deprotonated by NaNH2 in liquid NH3? 3-Methylhex-2-yne Pent-2-yne 3-Methylbutyne none of these Hex-3-yneAssume that 2-chloropropane reacts with CN− in an SN2 reaction. Use the JSME editor () to draw the structure of the substitution product of the reaction. The guide on how to draw your structure can be found here Important Note: When drawing the structures in the JME editor please adhere to the following formats: 1. If the nucleophile is OH−, DO NOT manually add the "H" to the final product 2. If the nucleophile is CN−, be sure to include the appropriate bonding between the C and N in the final product
- What are ALL of the products of buta-1,3-diene and bromine water? I know how to get to the major product (bromine and OH both to the left of the double bond) but don't know how to get to the minor product (bromine to the left, OH to the right)?Consider the synthesis scheme in Figure 12. Draw the structure of B. [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).] *A hydrocarbon of unknown structure has the formula C8H10. On catalytichydrogenation over the Lindlar catalyst, 1 equivalent of H2 is absorbed. Onhydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed.(a) How rnany degrees of unsaturation are present in the unknown?(b) How many triple bonds are present?(c) How many double bonds are present?(d) How many rings ar e present?(e) Draw a structure that fits the data.
- i need help filling out the following SN2 reactions with appopiate reactants, products, or reagents,I have this task in organic chemistry (book: Brown's introduction to organic chemisty, global edition). Task 10:42. In (a) I have to tell what the funcion of K2CO3 is in step 1. Is it that CO32- take the hydrogen atom in 1-napthol? Will it then be a SN2 mechanism? In (b) I have to name the amine used in step 2 to form Propanolol. But I can't really find out how to come up with an amine that will make that reaction. Here are two pictures of the task:Finish the synthesis by listing out the reagents/solvents used and draw intermediate structures. Want solution ASap