What are the organic products formed in each reaction? 11 C - C=C - c -C + Br -> 12 C-c -c -c=C + NBS 13 + Cl2 L) 14 uv C -( -c=c + H Br av 15 C -C =c - c -c +HBr J-リ-0
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- What is the stereochemistry of the product made by the reaction of but-2-yne with 1 equivalence of H-Br? CH3 - C ≡ C - CH3Cyclohexene plus 1) Hg(OAc)2, H2O; 2) NaBH4; yields __________. HO2CCH2CH2CH2CH2CO2H a cyclic diketone cyclohexyne cyclohexanol OHCCH2CH2CH2CH2CHOFor each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2) hydroboration–oxidation.(a) hex-1-yne (b) hex-2-yne
- The stereochemistry of the products of reduction depends on the reagent used, with this in mind, how would you convert 3,3-dimethylbutan-2-one [CH3COC(CH3)3] to: (a) racemic 3,3-dimethylbutan-2-ol [CH3CH(OH)C(CH3)3]; (b) only (R)-3,3- dimethylbutan-2-ol; (c) only (S)-3,3-dimethylbutan-2-ol?Draw all products of the reaction of (1S,2R)-1-bromo-1,2-dimethylcyclohexane in 80%H2O/20%CH3CH2OHat room temperature..Which substituent is the strongest deactivator to EAS reactions? -NO2 -Cl -CH3 -OH
- (CH3)3CCH=CHCl (1)NaNH2 -----> (2)H2O Which of the following is the product for the given reaction? a) (CH3)3CCH≡CH b) (CH3)3CCH=CH2 c) (CH3)3CCH=CHOH d) (CH3)3CCH=CHNH2Predict the major product(s) for each reaction. Include stereochemistry where appropriate.(a) 1@methylcyclohexene + Cl2>H2O (b) 2@methylbut@2@ene + Br2>H2O(c) cis@but@2@ene + Cl2>H2OFor each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2) hydroboration–oxidation.(a) hex-1-yne
- N(CH2CH3)3 + HNO3 --------> a.) rewrite the reaction using bond-line structure of reagents and products of the reaction b.) supply the curved arrows explaining the mechanism of the reactionThe reaction of 2-ethyl-1-pentene with Br2, with H2 + Pd/C, or with R2BH/THF followed by aqueous HO- + H2O2 leads to a racemic mixture. Explain why a racemic mixture is obtained in each case.6 H + + 6 I- + ClO3- → 3 I2 + 3 H2O + Cl- Which oxidizing reagent is in this reaction?