Rank the carbocations in the table below in order of increasing stability (1 least stable and 4 most stable). Give detailed Solution with explanation needed of all with structures don't give Handwritten answer + F F + + (Choose one) (Choose one) (Choose one) (Choose one) A
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- Chemistry 3. Complete the following reaction scheme. Give all product(s) and indicate major or minor and any relevant stereochemistry. (а) NaOEt heat (b) heat (c) Br NaCN DMF (d) (e) OH H,SO,/H,PO, heat (f) HBr (g) 1) BH. THE 2) H,0, OH (h) 1) Hg(OAC), H-0 2) NaBH, (i) KMNO, NaOH ColdOrder these according to decreasing stability; 1 being the most stable, 4 the least stable. A B C D(-)-Cameroonanol has been isolated from the essential oil of Echinops giganteus (globe thistle) plants and it is associated with a strong woody fragrance. Its structure, includ- ing relative stereochemistry, was confirmed when it was made in the laboratory according to the sequence shown below.' Recall that a C=C bond is made up of one o bond and one 7 bond. These two bonds together have a combined BDE (bond dissociation energy) of 607 kJ/mol. Use this information to estimate the AH for the conversion of compound 1 into compound 2. Br two steps .... H HBr hv H.. (--Cameroonanol
- (c) Arrange the following species in order of increasing stability. Explain. CH, H,C- -CH, CH, H,C-HC `CH H,C- `CH, HČ- -CH,Arrange the following in increasing order of stability:Q3. 2-Bromopentane, when treated with alcoholic KOH yields a mixture of three alkenes A, B and C. Identify A, B and C. Which is predominant? Q4 Which statement below about Sn1 reactions is incorrect? (A) SN1 reactions are stepwise and have intermediates. (B) The slow step in a SN1 reaction is formation of the carbocation intermediate. (C) SN1 reactions have first order kinetics which means only the alkyl halide is involved in the rate limiting step. (D) The products of a SN1 reaction will be a pair of enantiomers. (E) An aprotic solvent is best for Sn1 reactions as they tend to help stabilize carbocation intermediates.
- Rank the carbocations in the table below in order of decreasing stability (1 most stable and 4 least stable).Q4 Which statement below about Snl reactions is incorrect? (A) SNl reactions are stepwise and have intermediates. (B) The slow step in a Snl reaction is formation of the carbocation intermediate. (C) SNl reactions have first order kinetics which means only the alkyl halide is involved in the rate limiting step. (D) The products of a Syl reaction will be a pair of enantiomers. (E) An aprotic solvent is best for Snl reactions as they tend to help stabilize carbocation intermediates.(c) Arrange the following species in order of increasing stability. Explain. CH, H,C- -CH2 CH3 H;C-HC `CH; H,C- CH3 -CH2 A B
- Arrange the following carbocations in order from least to most stable. First, expand the structures to show all of the carbon and hydrogen atoms, at least in the vicinity of the charge. +Please help with 4c, 4d, and 4e. We havent learned kaw of equivalents so please do 4c a different way. thank youQ.1. : Name the following compounds. Specify stereochemistry, if applicable. a) Х b) S НО ОН Br ОН ОН I