56. Compound X (C;H12) is hydrogenated in the presence of Pd/BASO4 to produce (Z)-2-methyl- 3-hexene. What is the structure of X? the tansfor b. 2-methyl-3-hexyne low! a. 2-methyl-4-hexyne c. 2-methyl-4-hexene d. 2-methyl-4-hexane 57. How many meso compounds: CH3 CH Br Br CH3 CH b. 1 с. 2 d. 3 a. 0 58. Which of the following statements is (are) true for cis-1,2-dichlorocyclopropane? a. This compound is chiral. b. The enantiomer of this compound is trans-1,2-dichlorocyclopropane. c. This compound contains no asymmetric carbons. d. none of the above 59. Which structure provide (2R, 3S)-2-amino-3-hydroxybutanoic acid? он о он OH OH HO HO HO HO NH2 NH2 NH2 NH, D B

56. Compound X (C;H12) is hydrogenated in the presence of Pd/BASO4 to produce (Z)-2-methyl- 3-hexene. What is the structure of X? the tansfor b. 2-methyl-3-hexyne low! a. 2-methyl-4-hexyne c. 2-methyl-4-hexene d. 2-methyl-4-hexane 57. How many meso compounds: CH3 CH Br Br CH3 CH b. 1 с. 2 d. 3 a. 0 58. Which of the following statements is (are) true for cis-1,2-dichlorocyclopropane? a. This compound is chiral. b. The enantiomer of this compound is trans-1,2-dichlorocyclopropane. c. This compound contains no asymmetric carbons. d. none of the above 59. Which structure provide (2R, 3S)-2-amino-3-hydroxybutanoic acid? он о он OH OH HO HO HO HO NH2 NH2 NH2 NH, D B

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 7E: When toluene is treated with sulfuric and nitric acids under special conditions, three nitro (NO2)...

See similar textbooks

Similar questions

A hydrocarbon of unknown structure has the formula C8H10. On catalytichydrogenation over the Lindlar catalyst, 1 equivalent of H2 is absorbed. Onhydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed.(a) How rnany degrees of unsaturation are present in the unknown?(b) How many triple bonds are present?(c) How many double bonds are present?(d) How many rings ar e present?(e) Draw a structure that fits the data.
help ASAP Draw the products formed when cyclohexene is treated with this reagent: NBS (aqueous DMSO)
What is the product of the reaction shown in Image 26? a. cis-2,3-epoxybutane b.racemic (2R,3R) and (2S,3S)-2,3-butanediol c. CH3CH=O d. meso-2,3-butanediol meso-2,3-butanediol
Name (including E/Z stereochemistry) the five alkenes that can produce 3-bromo-3-methylhexane on reaction with HBr. Draw the skeletal structure of each molecule.
KMnO4, warm, conc'd reacts with hept-1-ene to yield __________. CO2, hex-1-ene CO2, hexanoic acid Formic acid, pentanoic acid Ethanoic acid, pentanal Formic acid, hexanone
How will you convert:(i) Propene to Propane-1-ol?(ii) Ehtanal to Propan-2-ol
Draw the one most stable alkene that is formed when the structure shown below is heated with H₃PO₄. .
Which structure will not yield cis- or trans- isomers after a reaction with H2/Lindlar catalyst or Na/NH3?
Draw all products of the reaction of (1S,2R)-1-bromo-1,2-dimethylcyclohexane in 80%H2O/20%CH3CH2OHat room temperature..
The stereochemistry of the products of reduction depends on the reagent used, as you learned in Sections 20.5 and 20.6. 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?
Give the structure corresponding to each name. a. (E)-4-ethylhept-3-ene b.3,3-dimethylcyclopentene c.4-vinylcyclopentene d.(Z)-3-isopropylhept-2-ene e.cls-3,4-dimethylcyclopentene f.1-isopropyl-4-propylcyclohexene g.3,4-dimethylcyclohex-2-enol h.3,5-diethylhex-5-en-3-ol
Consider a reaction where cis-but-2-ene is treated with a peroxy acid followed by OH- /H20. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.