As we know in Sn1 mechanism,carbocation intermediate will form. As the stability of carbocation increases reactivity towards Sn1.
(A) is correct option.
I form most stable carbonation due to resonance.
23. What is the correct order of increasing reactivity for these substrates under Sn1 conditions? A)...
23. What is the correct order of increasing reactivity for these substrates under Sn1 conditions? A) III < IV <]<1 B) IV < || < IV <1 I II IV C1<]I < III < IV D) IV < || <I< III
Arrange the following compounds in an increasing order from the least acidic to the most acidic. COOH O III < IV < | < || O ll < III < | < IV 01 < III < IV < || None of the choices. O ll < III < IV <
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 bonds from smallest wavenumber to largest wavenumber: 1.C-O II. C=0 II. CEN IV. C=C 1.1V<l<lll<ll 2.]<ll<IV<III 3.I<IV<ll<lll 4. II<IV<Ill</ QUESTION 5 Identify the structure that fits best the spectrum provided: - TRANSMITTANCE [%] 6080 40 WAVENUMBER [cm-1] MNH2 OH HN А в 1. A 2. B 3.C 4.D 5. E
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
1.) What is the order of reactivity of the following reagents under SN1 conditions? Under SN2 conditions? Draw the structures of each using the bond line method and explain your answers. 1-methyl-1-bromocyclohexane, 1-bromopropane, 2-bromohexane 2.) What is the order of reactivity of the following reagents under SN1 conditions? Under SN2 conditions? Explain your answers. CH3CH=CHBr, CH3CH=CHCH2Br, CH3CH2CH2Br 3.) We did not use crotyl chloride in this experiment. However, based on your knowledge of SN1 and SN2 predict the behavior of...
Question 28 Rank the below substituted cyclohexanes by increasing relative stability. (least stable first) F I<ll<III OO ll<l<III Ill<ll</ Il<llll
18. Arrange these compounds in order of increasing boing point: t. 1-butanol I. Butanal II. propanoic acid a) I<II< III b) II <I< III
Rank the following compounds in order of increasing acidity, putting the least acidic compound first. 1) III < 1 < || < IV O 2) IV < < || < III 03) 111 < || <I< IV 4) || < IV <1 < III
of the choices below, which gives the order for Increasing first ionization energies? Select one: a. Li <B< Be <C<O<N b. Li <Be <B<C<O<N o c. Li < B < Be <O<C<N d. Li < Be <B<C<N<O O e. Li <B<Be <C<N<O Oo oo