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- Draw a structural formula for the product formed upon hydroboration/oxidation of the alkene below. CH;CH2CH,CH2 C=CHCH3 CH;CH,CH,CH20 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?Draw the structures of the following molecules: (a) trans-l-Bromo-3-methylcyclohexane (b) cis-1, 2-Dimethylcyclobutane (c) trans-1 -tert-Butyl-2-ethylcyclohexane
- 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.Chemical Reactions: Give the product/s of each chemical reaction 1. Reaction of this alkene to the different reagents written above and below the arrows. ¡ HBrWhich is not an alkene formed when 2-chloro-2-methylbutane is dehydrohalogenated with NaOCH2CH3 (sodium ethoxide)? O 2-methyl-but-2-ene O 1-methylcyclobut-1-ene 2-methyl-but-1-ene
- Determine the product of the reaction: CH2-0-č-(CH2)1«CH, CH-0-č-(CH2hCH=CH(CH2),CH, + 3 NAOH CH;-0-č-(CH2le(CH2CH=CH)2(CH2),CH, O=O OGive the major product(s) of the following reaction. CH3CH2CH=CH2 ? CI (1 mole) HF, heatDraw the organic product(s) formed upon the addition of HBr to (a) 2-methyl-2-pentene, (b) trans-2-hexene, and (c) 4-methylcyclohexene. How many regioisomers can be formed in each case?
- 2. Name and draw the product produced by the oxidation of each compound. (а) CH,— CH,—CH,— CH—СH,—он ČH2-CH3 ОН (b) CH,— CH—CH, — CН,— СH, —СH, (с) CH3-CH2-CH2-C-HDraw a structural formula for the missing organic product in the reaction below. + CH;CH,NHCH2CH3 CH3CH2CH2CH2CH,COCCH,CH2CH,CH,CH3 CH;CH,CH,CH,CH2COHO2 can oxidize 4-tert-butylcatechol, and gives the structure of the oxidized product. How many carbon and oxygen atoms (total) of 4-tert-butylcatechol are actually etting oxidized? Please explain how!