Which of the following has two equatorial alkyl substituents in its most stable conformation? (a) 1,1-dimethylcyclohexane (b) cis-1,2-dimethylcyclohexane (c) cis-1,3-diethylcyclohexane (d) cis-1,4-diethylcyclohexane

Which of the following has two equatorial alkyl substituents in its most
stable conformation?
(a) 1,1-dimethylcyclohexane
(b) cis-1,2-dimethylcyclohexane
(c) cis-1,3-diethylcyclohexane
(d) cis-1,4-diethylcyclohexane
by

1 Answer

Answer :

cis-1,3-diethylcyclohexane
by

Related questions

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‘Lock’ and ‘Key’ model of enzyme action proposed by Fisher implies that (A) The active site is flexible and adjusts to substrate (B) The active site requires removal of PO4 group (C) The active site is complementary in shape to that of the substrate (D) Substrates change conformation prior to active site interaction

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Fischer’s ‘lock and key’ model of the enzyme action implies that (A) The active site is complementary in shape to that of substance only after interaction. (B) The active site is complementary in shape to that of substance (C) Substrates change conformation prior to active site interaction (D) The active site is flexible and adjusts to substrate

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Among Cis and Trans structure of Hex-2-ene which has higher boiling point and why?

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Predict which of the following alkenes reacts the fastest with HCl? (a) CH3CH2CH2CH2CH=CH2 (b) cis-CH3CH2CH=CHCH2CH3 (c) trans-CH3CH2CH=CHCH2CH3 (d) (CH3)2C=CHCH2CH3

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What is(are) the product(s) in the Pd-catalyzed hydrogenation of 1,2- dimethylcyclopentene? (a) trans-1,2-dimethylcyclopentane (b) cis-1,2-dimethylcyclopentane (c) a mixture of trans and cis-1,2-dimethylcyclopentane (d) 1,1-dimethylcyclopentane

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What is the product when 3-heptyne reacts with the Lindlar catalyst? (a) 2-methyl-2-heptene (b) trans-3-heptene (c) cis-2-methyl-3-hexene (d) cis-3-hexene

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The reagent needed to convert 2-butyne to cis-2-butene is : (a) H2/Pt (b) H2/Lindlar’s catalyst (c) Li/NH3 (d) Na/NH3

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Rank the following dienes in order of increasing stability : trans-1, 3-pentadiene, cis-1,3-pentadiene, 1,4-pentadiene and 1,2-pentadiene

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Which of the following statements about propene, CH3CH=CH2, is correct? (a) All nine atoms lie in the same plane. (b) The compound has a cis and trans isomer. (c) There is a total of eight sigma bonds. (d) All the carbon atoms are sp2 hybridized

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Which of the following compounds will have zero dipole moment? (a) cis-1,2-dibromoethylene (b) 1,1-dibromoethylene (c) trans-1,2-dibromoethylene (d) all of these

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Why do trans isomers of alkenes have lower boiling points than cis isomers? (a) trans isomers have better symmetry (b) cis isomers have better symmetry (c) trans isomers are less polar (d) cis isomers are less polar

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How do the melting points of trans isomers compare to the cis isomers for alkenes? (a) cis isomers have higher melting points (b) trans isomers have higher melting points (c) both have similar melting points (d) no consistent trend is observed

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Which of the statements is false regarding chiral compounds? (a) rotate the plane of polarized light (b) have cis and trans isomers (c) exist as enantiomers (d) can be detected with a polarimeter

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Which of the following compounds may exist as cis-trans isomers? (a) 1-Butene (b) 2-Butene (c) Cyclopropane (d) Acetone

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What is the name given to the non-superimposable mirror image forms of chiral compounds? w) cis-trans x) enantiomers y) functional isomers z) diasteriomers

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