In these reactions, indicate the products M and N that are obtained (draw the formulas). Comment on each reaction briefly. O2N-CH3 + EtO-Na+, EtOH, 3 equivalents + CH2=CH-COOCH2CH3 → M (16 Carbons) M (16 Carbons) + H2 / Ni Raney → N (14 Carbons)
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- Write down the common (not IUPAC) names of the organic molecules that would be released if this molecule were hydrolyzed: CH2−O−C—(CH2);–CH=CH–CH2–CH=CH—(CH2)4—CH3 CH-O-C-(CH2)14-CH3 O 11 CH2−O−C— (CH2)14 — CH3 Separate each name with a comma. You will find useful information in the ALEKS Data resource. 1 010 Continue O a X 000 Y F8 F9 Submihw 7 helpWrite down the common (not IUPAC) names of the organic molecules that would be released if this molecule were hydrolyzed: CH,—O—C—(CH2)—CH=CH-CH,—CH=CH—(CH2) — CH3 CH-0- -(CH2)–CH=CH(CH2)CH3 O CH,—O-C=(CH2)=CH=CH(CH2)—CH3 Separate each name with a comma and a space. You will find useful information in the ALEKS Data resource. type your answer...
- When 2-pentene is treated with Cl2 in methanol, three products are formed. Account for the formation of each product (you need not explain their relative percentages).Provide the reactants (starting material), reagents, or products to complete the following reaction equations. ✓ + Cl₂ dichloromethane + Br2 H₂O Br₂ Br лоH Provide the reactants (starting material), reagents, or products to complete the following reaction equations. ~ + Cl₂ dichloromethane, +Br₂ H₂O Brz Br. Лонorganic chemistry help Fill in the missing starting materials, reagents, or major products of each reaction
- Determine the one or two steps it takes to get from the starting material to the product using the reactions found in this chapter. HC-C HO, a. HC, HO CH2-OH b. СH, — CH—СH,—CH—CH, ČH,-CH3 CH2 || CH3-CH-CH,-Ĉ-CH3 ČH,-CH3 Br c. CH;-CH,-C=CH2 CH,-CH,-C-CH; ČH3Use the following reagent table for the reaction of: cyclohexanol + H2 SO4 → cyclohexene Chemical MW (g/mol). Density (g/mL) mmols used Amount used cyclohexanol 100.16 0.9624 1.50 mL Sulfuric Acid 98.08 1.83 1.00 mL cyclohexene 82.14 Based on your answers in the previous two questions, identify what the Limiting Reagent for the reaction is:An important step in one synthesis of carboxylic acids is the deprotonation of diethyl malonate and its alkyl-substituted derivative: Base CH;CH2O OCH,CH3 CH;CH,0 OCH2CH3 H2 Diethyl malonate Base CH;CH,0 °C `OCH,CH3 CH;CH,O OCH,CH3 R Alkyl substituted diethyl malonate NaOH can deprotonate diethyl malonate effectively, but NaOC(CH3)3 is typically used to deprotonate the alkyl-substituted derivative. Explain why.
- Acid-catalyzed dehydration of secondary and tertiary alcohols proceeds through an E1 mechanism. The first step is the protonation of the alcohol oxygen to form an oxonium ion. Dehydration of 3-methyl-2-butanol forms one major and two minor organic products. Draw the structures, including hydrogen atoms, of the three organic products of this reaction. н н :бн н Нас. Нас. CHз CH3 ČH3 CH3 3-methyl-2-butanol an oxonium ion Major Product Minor Product Minor ProductComplete the reaction by providing the starting material/reagent/products. Match each item to a choice: CI Cl₂ FeCl3 HO OH NO₂ for HO NO₂ O SO3 conc. H₂SO4 NO₂ KMnO4 H₂OFinish the indicated reaction by filling in and starting materials, reagents or products as needed