Ans- B < E < C < A < D
Explanation-
Heat of Hydrogenation is the change in Enthalpy for hydrogenation of alkene. We know in hydrogenation process, an unstaturated Hydrocarbon (here Alkene) is converted into a saturated hydrocarbon (an Alkane). Now generally heat is released in this process.
Now more stronger an alkene is, less is the amount of heat released. Or we can the strength of alkene and Energy of hydrogenation is inversely proportional.
Thus stronger the alkene (here diene), lesser is the Heat of Hydrogenation and vice versa.
Now the rules followed in determineing the stability of diene is-
i) Conjugated dienes (double bonds are present alternate to each other) are more stable than other dienes
So here conjugated dines (in B and E) are more stsable than the rest
ii) Now more substituted dines (more groups attached at the douby boned C-atoms) are more stable than less substitued alkenes.
So here between B and E, (B is more stable) as the last end of B us more substituted.
And between A and C, (C is more stable)
iii) Between regular diene and allene (compound D) allenes are the least stable.
So here the compound D is the least stable among all.
Thus the decreasing order of diene stablity in the given compounds will be-
B > E > C > A > D
The the increasig order of Heat of Hydrogenation wiil be as (less stable, more Heat of Hydrogenation)
B < E < C < A < D
Rank the following compounds in order of increasing heat of hydrogenation. A B D E OB<C<E<A<D...
Rank the following compounds in order of increasing heat of hydrogenation. A C D E OD<A<C<E<B B<E<C<A<D O E<B<C<A<D OD A<E<C<B OB<C<E<A<D
4 pts Rank the following compounds in order of increasing heat of hydrogenation. you А B C D E OD<A<C<E<B OB<E<C<A<D O E<B<C<AD OD A<E<C<B OB<C<E<A<D Rank the following in order of decreasing heat of combustion. А B D E OB>E>C>A>D OD > A >C>E>B OB>C>D>A>E O E>B>C>A>D O E>A>D>C>B
Rank the following compounds in order of increasing acidity based on the explicit hydrogen shown. F F CH H H H А B С D E O C<B<A<C<D OB<D<E<A C OB<E<D<A C O CA<D<E<B OB E<A<C<D
Rank the following compounds in order of increasing acidity, putting the least acidic first. O Онон ва -OH 1) ill < || < IV <1 O2) ||| < IV< II </ 3) 1 < IV < || < III 4) 1 < || < III < IV
Rank the following compounds in order of increasing strength of intermolecular forces: CH3NH2, CH3CH3, CH3Cl A) CH3Cl < CH3CH3 CH3NH2 C) CH3NH2 CH3C CH3CH3 CH3Br, CH3l, CH3Cl D) CH3Cl CH3Br < CH3l E) CHalCH,CI CH,Br
explain reasoning Rank the following in order of increasing reactivity for nucleophilic addition D<A<B<C O C<A<B<D D<C<B<A O C<B<D<A Given the reaction below, check ALL the statements that are true. * mCPBA O The reaction is called Baeyer Villiger Reaction It is a mild oxidation of ketone that forms esters The product formed is correct
The answer is given. Please help understand why ! Rank the following compounds in order of increasing stability (least to most stable answer this question, think of why (give reasons) one molecule is more or less stabl another. LEAST) C<B<D<A (MOST)
Rank the following bonds in order of increasing bond polarity. A) 1 <2<3 B) 1< 3 < 2 C)3 < 1<2 D)3<2<1 E) 2 <3 < 1
Rank these radicals from least to most stable. O A<B<C O A<C<B OB<A<C OB<C<A Ò C<A<B OC <B<A
Rank the following compounds in order of increasing acidity, putting the least acidic first. alon F. ОН Br ОН ОН ІІ ІІ IV ОІ<IV <<Ш ОІ<< < IV ОШ <II <IV <I OIH <IV <II <I