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The expected product(s) resulting from addition of Br2 to (E) -3-hexene would be:


A) a meso dibromide.
B) a mixture of optically active enantiomeric dibromides.
C) a mixture of optically inactive enantiomeric dibromides.
D) (Z) -3,4-dibromo-3-hexene.
E) (E) -3,4-dibromo-3-hexene.

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The Markovnikov product,resulting from an addition reaction to an unsymmetrical alkene,is formed because:


A) the product is statistically favored.
B) steric hindrance favors its formation.
C) the reaction proceeds via the more/most stable carbocation.
D) the reaction forms the more/most stable product.
E) All of the above are valid reasons

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A reaction that could potentially yield two or more constitutional isomers,but as in hydroboration-oxidation produces only one isomer,is said to be _____________________.

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The expected Markovnikov addition product of HI to 2-methyl-2-butene is:


A) 2-iodopentane
B) 2-iodo-2-methylbutane
C) 1-iodo-2-methylbutane
D) 2-iodo-1-methylbutane
E) 3-iodo-2-methylbutane

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In a reaction where addition and elimination reactions are in competition,which of the following statements is most correct?


A) Addition and elimination reactions are favored at low temperatures.
B) Addition and elimination reactions are favored at high temperatures.
C) Only addition reactions are favored at low temperatures.
D) Only elimination reactions are favored at low temperatures.
E) Addition and elimination reactions are disfavored at low temperatures.

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For an addition reaction,why does the free energy term, Δ\Delta G,become more positive with increasing temperature?


A) The positive entropy term dominates at high temperature.
B) The negative entropy term dominates at high temperature.
C) The positive enthalpy term dominates at high temperature.
D) The negative enthalpy term dominates at high temperature.
E) The enthalpy and entropy terms cancel at high temperature.

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What is the IUPAC name of the expected major product formed upon reaction of HCl with 3-methyl-1-butene?


A) 1-Chloro-2-methylbutane
B) 1-Chloro-3-methylbutane
C) 2-Chloro-2-methylbutane
D) 2-Chloro-3-methylbutane
E) 1-Chloropentane

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Which of the following alkene addition reactions occur(s) specifically in syn fashion?


A) dihydroxylation using OsO4,H2O2
B) addition of H2
C) hydroboration
D) addition of HCl
E) A,B,and C

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The regioselectivity and stereospecificity in hydrohalogenation of an alkene is best described as:


A) Markovnikov orientation with syn-addition
B) Markovnikov orientation with anti-addition
C) anti-Markovnikov orientation with syn-addition
D) anti-Markovnikov orientation with anti-addition
E) Markonikov orientation with both syn- and anti-addition

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Addition reactions of alkenes are characterized by:


A) formation of a π bond
B) addition of two groups across a double bond
C) breaking of a π bond
D) A and B
E) B and C

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For the complete reduction of 1 mole of (3E,5E) -hepta-1,3,5-triene with H2 using a Pd catalyst,how many moles of H2 are consumed?


A) 1
B) 2
C) 3
D) 4
E) 5

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Which of the following will yield 2-methylpentane upon catalytic hydrogenation?


A) 2-methyl-1-pentene2
B) 2-methyl-2-pentene
C) 4-methyl-2-pentene
D) 4-methyl-1-pentene
E) All of the above

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π\pi bonds are quite susceptible to reaction with electron-seeking reagents,also referred to as ____________________.

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How many moles of hydrogen (H2) are consumed in the catalytic reduction of 1 mole of 1,3-dibromocyclohexa-1,4-diene?


A) 12
B) 2
C) 3
D) 4
E) None of the above

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The regioselectivity and stereospecificity in the acid-catalyzed hydration of an alkene is best described as:


A) Markovnikov orientation with syn-addition
B) Markovnikov orientation with anti-addition
C) anti-Markovnikov orientation with syn-addition
D) anti-Markovnikov orientation with anti-addition
E) Markonikov orientation with both syn- and anti-addition

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What product is formed when trans-1,2-dimethylcyclohexane is reacted with Pd/C and H2?


A) No reaction
B) cis-1,2-dimethylcyclohexane
C) trans-3,4-dimethylhexane
D) trans-1,2-dimethylhexane
E) None of the above

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When an alkene is subjected to treatment with Hg(OAc) 2 in alcohol,followed by reaction with NaBH4,what functional group is formed?


A) ether
B) epoxide
C) alkane
D) syn diol
E) alkyne

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Addition reactions are favorable at low temperatures because:


A) the positive enthalpy term is larger than the negative entropy term.
B) the negative enthalpy term is larger than the positive entropy term.
C) the positive enthalpy term is smaller than the negative entropy term.
D) the negative enthalpy term is smaller than the positive entropy term.
E) the enthalpy and entropy terms are equal.

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Which of the catalysts listed are used in the homogenous catalytic hydrogenation of alkenes? I) Ni II) Pt III) Wilkinson


A) I
B) II
C) III
D) I and II
E) II and III

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The decrease in entropy (the Δ\Delta S value is negative) observed for alkene addition reactions results from:


A) the breaking of a π and σ\sigma bond.
B) the formation of two σ\sigma bonds.
C) the reaction being exothermic.
D) two molecules reacting to form a single molecule.
E) the temperature dependence of the Δ\Delta S term.

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