alkenes Flashcards

(15 cards)

1
Q

products formed from complete combustion with alkenes

A

co2 and h2o

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2
Q

why are alkenes not used as fuels

A

presence of c=c bonds in alkenes make them more useful as starting material for manufacturing other important chemicals

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3
Q

function of pi electrons in ensuring that alkenes are reactive in c=c bond

A

attract electrophiles or induce dipole in approaching molecules to form electrophiles.

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4
Q

what is the product formed from the addition of halogens to alkenes, reagents and conditions, observations

A

dihalogenoalkanes, halogen in organic solvents at room temp, orange-red bromine decolourises

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5
Q

describe briefly electrophilic addition mechanism for alkenes

A

pi bond in alkene approaches the halogen and induces a dipole. The halogen atom with partial positive charge acts as an electrophiles.

The pi electrons in the c=c bond act as the nucleophile and approaches the partial positive halogen atom to form an unstable carbocation immediate and a halide ion.

The halide ion attacks the carbocation intermediate to form the dihalogenoalkane.

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6
Q

product formed from addition of halogens in water, and reagents and conditions, observations

A

halohydrins, aqueous halogen at room temp, orange bromine water decolourises

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7
Q

products formed, reagents and conditions as well as observations in the addition of hydrogen halides

A

halogenoalkanes, dry HX(g), at room temp, no observable change

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8
Q

why is the rate of reaction highest for HI, and lowest for HCl

A

HI has longest bond length, weakest bond strength, rate of reaction fastestm

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9
Q

explanation behind markonikov’s rule

A

electron donating effect of alkyl groups help to stabilize carbonation by dispersing the positive charge of the carbon atom. a carbonation with more alkyl groups more stable, and forms at a higher rate. more stable carbonation leads to major prod.

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10
Q

addition of steam to alkenes (hydration) product reagents and conditions, observations

A

alcohol, h2o(g), heat in presence of concentrated h3po4 catalyst at high temp and pressure, no observable change

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11
Q

reduction (catalytic hydrogenation) product reagents and conditions, observations

A

Hydrogen Gas and Ni Catalyst, product: alkanes, no observable change

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12
Q

mild oxidation product reagents and conditions, observations

A

product: diols
cold, alkaline KMnO4
observation: Purple KMnO4 decolourises, Brown Precipitate of MnO2 is formed

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13
Q

srong oxidation product(s) reagents and conditions, observations

A

products: carbon dioxide and water, carbonyl compounds or carboxylic acids

acidified KMnO4, heat under reflux

observation: purple KMnO4 decolurises

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14
Q

dehydration product(s) reagents and conditions, observations

A

alkene, H2O(g), conc H3PO4 catalyst, heat

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15
Q

dehydrohalogenation product(s) reagents and conditions, observations

A

alkene, halide ion, H2O(g), NaOH in ethanol, heat under reflux

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