Which of the following compounds could be separated from the others using an extraction procedure? 167 HO. 34.6 C 80.1 °C 110 6 C 118.1 °C O benzene acetic acid Otoluene Google diethyl ether
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- Write 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...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 Submi0 CH₂ → ?? If the above compound is subjected to combustion, what are the products? ethanoic acid +2-phenyl-ethene-1-ol 15CO₂ (g) + 5H₂0 (g) O 2-phenyl-ethyl-ethanoate + H₂O 20CO₂ (g) + 10H₂O(g) →?? CH, if the above compound was treated with H and H₂O what product will form?
- The following chemical reaction is used to synthesize a flavouring agent that has an aroma similar to bananas. H₂SO4(aq) CH3COOH(1) + CH₂(CH₂)₂OH(1) I || Identify the type of reaction that is represented by this synthesis. Select one: O hydrogenation O esterification O addition O substitution O elimination Identify the functional group and the IUPAC name for each of the three compounds in the reaction below: H₂SO4(aq) I Compound Functional Group IUPAC Name II CH₂COOH(1) + CH₂(CH₂)₂OH(1) I || III CH3COO(CH₂)₂CH₂(1) + H₂O(1) III IV ◆ → ◆ CH3COO(CH₂)₂CH₂(1) + H₂O(1) IV ||| ◆ ◆A solid sticky substance which strongly repels water is made of the following molecules: CH3 (CH2)5 — || (CH2)14-CH3 If it is treated with sulfuric acid and heat, two new substances can be recovered. One is an alcohol. Write the chemical formula of the alcohol. Give the common (not IUPAC) name of the other substance. 0A Grignard reagent will react with formaldehyde to form a primary alcohol, an aldehyde to form a secondary alcohol, and a ketone to form a tertiary alcohol. Identify the product formed from the reaction shown. i Η + CH3CH2CH2MgBr ? The product is: OH H OH OH O H OH
- Draw the structures of two alkenes that would react to form the alcohol below by acid-catalyzed hydration. Your alkenes should be different regioisomers that yield the alcohol as the major product without requiring rearrangement. 1 0 :0 s + I. X H₂SO H₂O ОНArrange the following substances in order of increasing boiling point: CH:CH20H, НОСH-CH2OH, СH;CH-CI, and CICH2CH-0H CH CH2OH < СICH-CH2OH < CH3CH2CI < HОСН2CH2ОH CH CH-CI < CHЗCH2ОH < CІCHCH2ОH < НОСН2CH2ОH CH3CH2OH < CH;CH2CI < HOCH2CH2OH < CICH2CH2OH CH3CH2OH < HỌCH2CH2OH < CH3CH2CI < CICH2CH2OHThe reaction shown below does not give the product indicated. Which of the following best explains the error? 0 H₂. Pd/C Ethanol OH The reagent would react with both alkene groups, but not the carbonyl group as shown. The reaction has the arrow drawn in the wrong direction (reactants and products should switch places). The reagent does not react with alkenes, there would not be any reaction O The product should have no pi bonds.
- CH3COOH + 2H2 = C2H5OH + H2O %3D Acetate Ethanol Acetate may be hydrogenated to ethanol in industrial reaction systems using several catalysts: Select the most effective catalyst for this reaction system if the free energy of the reaction is -34 kJ/mol; Catalist effective at the temperature range 37-45°C, O Catalist effective at the temperature range 40-55°C, O Catalist effective at the temperature range 60-72°C,Choose the reagents that can be used to achieve the following conversion. More than one reaction is required, and reactions from earlier chapters may be necessary. Reagents may be used more than once. CH3-CH2-C-CH3 CH3-CH=CH-CH3 H2SO4 H,SO, 1 2. 180°C 140°C (0) H2 3. 4 Pt H+ H20 5. 6. CH;OH H2SO, (Enter multiple answers as a comma-separated list.)Acetylsalicylic acid commonly inflammation, and acts as a blood thinning agent. A group of STEM students experimented technique. The following are the initial materials for the experiment: 5.00 g of pure salicylic acid, 7.14 sulfuric acid as catalyst. After successful synthesis, the group was able to collect 5.25 grams of Aspirin. (Atomic weights: C= 12 amu; H = 1 amu; O= 16 amu; density acetic anhydride = 1.08 g/mL) known as Aspirin is used to treat fever, on the synthesis of this compound using recrystallization of acetic anhydride and 8 drops concentrated %3D Chemical reaction involved: OH C-CH3 0-C-CH3 C-OH C-CH3 CH3-C-OH C-OH Acetic anhydride Acetylsalicylic acid (C 9H8O4) Acetic Acid Salicylic acid (C7H603) (C 4H603) (C 2 H402)