Please help! Circle the fastest reactant for each pair in the test and give rational reason....
please explain why!
11. (2 points) Circle the member of each pair that is more soluble in water. a) oethyl ether pentane b) OH 1-butanol OH ethanol OH d) acetone cyclohexanone
2. (10 points) For each pair circle the compound that will give cloudiness when treated with ZaCly/HCI (conc.) the fastest. biologo
Circle the compound in each pair that would react faster with the indicated reagent system. (0.6 pts) Nal, acetone SN2 NaOCH3, CH3OH E2 CH3CH2OH or Br CN SN1/E1
2. For each pair of molecules, circle the stronger acid and provide a reason for your decision. Use diagrams as well as words in your explanation (4 pts)
please help!!
praw the reactant required to produce each major product. Be sure to indicate the Walle! indicate the correst dereichemistry where appropria нс с Cl, CH CI, hv NH OCHS Kąco, (a base) then CH,BI 1. Na (metal) 2. butyl bromide OCH, 1. Brg, hv, CHCI HC- 2. methanolysis NH2 1. mesyl chloride, pyridine 2. NH3 1. TICI, py 2. H20 (hydrolysis) 1.TSCI, K2CO3 2. Nal (acetone) Page 5 of 8
Give the structure of the major organic product, reactant, or
catalyst in each incomplete equation.
(e to i) please thanks!
CHE R ethylcyclohexane HCl Naoh CH,OH, Et, Y CH14) (an isomer of Y) Hg (0Ac), Nabtle H2SO4 (8) "3,3-dimethyl-1-butene 44. THE KOH ale, a НІ Et, o (h) 1.3 ACETONE 2.2nº (the only product!) (HOA) (an isomer of D I (C6H12) NaHSO4 + ACETONE 1. Ha (Ach, ng 2. NaBHA, THE II (C8H14) 1. O 2.Z, HOA (an isomer of...
Please help with these
thanks
How could the pair of structures be distinguished using IR spectroscopy? List the diagnostic peaks that would be present or absent for each pair. The IR spectrum below is of one of the compounds shown. Circle structure that corresponds to the spectrum and label the peaks you used to make your choice.
REAC Give the structure of the MAJOR arganic product , reactant, or cataiyst in each incomplete equation. Mа Pод THE (a) -3-methyl-1-butene glGAch Na B Кон HI сHон, а (b) H2SO4 (вн THF Hао OH, 4 (c) НВ- Bre X Etzo x-CaHsBr (d) "isobutene a4 CHs CH3 Br Br Br Ha NaOH HCI ethylcyclohexane Et2O Y (CsH14 (an isomer of Y) 3,3-dimethyl-1-butene" HglOAc) Na 6i 04 МЕСI THF oton 1 HI (h) Кон ale, A LO3 EtO 1 (CaH12) H-...
Please explain clearly and give the direct answer
Complete each reaction by giving the major product: Nal in EtOH solvent 11lll Melman Nal in acetone solvent EtOH in H2SO4 t-butyl alcohol (a) All Snl reactions occur with inversion of configuration. True or False (b) The rate-limiting step in a Syl reaction always yields a carbanion. True or False
Please help
The reaction below gives two S_N1 products. Draw them. Do not consider enantiomers. For each pair of molecules below circle the one that will undergo an S_N1 reaction the fastest. In class we discussed two possible mechanisms for the reaction below (see also section 8.6a of the text). Draw side-by-side reaction energy diagrams for each mechanism that clearly show the relative energies after each step. Give a curved arrow mechanism for the E1 reaction below. TFA (trifluoroacetic acid,...