Write down the common (not IUPAC) names of the organic molecules that would be released if this molecule were hydrolyzed: CH2 O Separate each name with a comma. You will find useful information in the ALEKS Data resource. CH2 O ༠༨༠༨༠༨ CH O ☐ α Y
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- Using your reaction roadmap as a guide, show how to convert ethylene into 1-butene. All of the carbon atoms of the target molecule must be derived from ethylene. Show all intermediate molecules synthesized along the way.X Upon ozonolysis, Compound X produces two compounds: Compound Y and Compound Z. Compound Y can also be prepared from the following synthetic route: PCC 1. R₂BH, THF 1. Mg. Et₂O PCC Compound Y 2. CH₂Cl₂ 2. NaOH, HO CH₂Cl₂ 3. H₂O* From this information, draw the structures of Compounds X, Y, and Z. For Compounds X and Z, different substituents are possible. For grading purposes, just use hydrogens as the substituents. Br مرد →] ►7 Which reagents and solvents can be used to synthesize (R)-2-cyanopentane from (R)-2- chloropentane? 8. Without changing reagent concentrations or amounts, what change could one make to the reaction shown below that would increase its reaction rate (explain your reasoning)? NaSCH2CH3 CH3CH2CH,CH,Br CH;CH,CH,CH,SCH,CH3 CH;OH
- Chemistry please help me answer the following questions. Draw a structure for the following compound: 2-Heptyne Draw a structure for the following compound: 2,2-Dimethyl-4-octyne D The transformation above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagent(s) in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. A B C D₂O NaOD NaNH, D E F NaD D₂. Lindlar's cat. D₂, PtIdentify the substitution products that form when 2-bromo-2-methylpropane is dissolved in a mixture of 80% ethanol and 20% water. a. Explain why the same products are obtained when 2-chloro-2-methylpropane is dissolved in a mixture of 80% ethanol and 20% water.Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CH3 CH3 H3PO4 HO, + H3C CH3 HO HO First stage in synthesis of the epoxy and polycarbonate ingredient bisphenol-A You do not have to consider stereochemistry. Include all valence lone pairs in your answer. In cases where there is more than one answer, just draw one.
- Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. CI H₂N OH • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na+, I, in your answer. • In cases where there is more than one answer, just draw one. Sn [F10. The Wolff-Kishner reaction, in which an aldehyde or ketone is treated with NH2NH2 and KOH, is: a) an oxidation c) an SN2 reaction b) a reduction d) a hydration 11. Which of these is most likely to dissolve in 5% NaOH? a) 1-decanol b) decanal c) decanoic acid d) 2-decanone 12. The following compound forms a cyclic hemiacetal all by itself. Draw the structure of that hemiacetal.Identify the reagents you would use to convert 1-bromopentane into pentanamide. 1-bromopentane → pentanamide The transformation above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. A. excess NH3 D. H3O+, heat G. Na₂Cr₂O7, H₂SO4, H₂O B. NaCN E. SOCI2 H. 1) LIAIH4; 2) H3O+ C. Mg F. NaOH I. PCC or DMP
- - How could the following changes in reaction conditions affect the rate of the reaction when isopropanol (IPA) reacts with 2-bromo-2-methylpentane? The concentration of the IPA is halved by adding petroleum ether as the solvent. b. The concentration of the bromoalkene is quadrupled. а.Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. 0 OH CI + H₂N • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na+, I, in your answer. In cases where there is more than one answer, just draw one. A ChemDoodle Activate WindowsConvert 2-pentanol into 2,3-dibromopentane. Draw structures of the starting material (2-pentanol) and final product (2,3-dibromopentane), and show the two reactions needed for this synthesis. Include the structure of the intermediate compound, and the reagents and conditions for each reaction. Then explain why 1,2-dibromopentane would not be a significant product of this synthesis.