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Why is the theoretical second product not formed in this reaction.
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- What is the product or reactant based on the information we are given down belowGiven the following table of bond dissociation energies (in kcal/mol), what is AH° for this reaction? (CH3);С —Н + Br -Br (CH);С — Br + Н—Br | CH3-H 105 (CH3)3C-H 91 CH3-Br 70 (CH3)3C-Br 65 Br-Br 46 H-Br 88 O +7 kcal/mol O -7 kcal/mol O +16 kcal/mol O -16 kcal/mol O cannot be determined with this informationCombine these two reactents in a way that they woul be separated when consumed. N OIH H + H - 0. (1 C
- What is the correct name for the compound below? O(25,35)-2-cyclopentyl-2,3-epoxyheptane (2R,3S)-2-cyclopentyl-2,3-epoxyheptane 1-butoxy-1-methylcyclopentane O(15,25)-1-methyl-1-cyclopentyl-1,2-epoxyhexane10. Draw a line structure for each organic product of the reaction shown below, including relevant stereochemistry. Do not draw multiple structures of the same compound. (6 pts) SN2 + HBr ???? OHNaming Alkenes 7-37 Name the following alkenes: (a) CH3 (b) CH3 CH2CH3 (c) CH2CH3 CH3CHCH2CH,CH CH3 H2C=CCH2CH3 CHCH2CH3 C=C H C=C H3C H3C H. H (f) H2C=C=CHCH3 (е) CH3 C=C (d) H H3C C=C CH3 C=C CH3 H3C H. H2C=CHCHCH CH3CH2CH2 CH3
- 6) Which products are, respectively, the kinetic and thermodynamic product? Br Br Br HBr (1 equiv.) 1. 2. 3.None5:10 34 7. Draw the structure of the intermediate (including stereochemistry, lone pair(s) and formal charge(s)) that forms when the alkene shown below (cis-3-hexene) reacts with Br₂ in an inert solvent. (4 pts) CH3 -CH3