10. Which of the following carbonyl compounds does not give 2-methylpentan-2-ol upon reaction with methylmagnesium iodide...
a) tert 14. Which of any alcohol upon reaction with methylmagnesium Which of the following compounds does NOT give a tertiary bromide? CH, HC CH₂ D - Η Β) 10. Which of the following compounds is NOT oxidized by pyridinium chlorochromate (PCC)? a) 2-methyl-2-butanol b) 1-pentanol c) 2-pentanol D) 1,3-propanediol 11. What is the complete systematic IUPAC name for the following compound? A) 4-(1-methylethoxy)-4-isopropyl-4-methylpent-2-cne B) 4-isopropyl-2,4-dimethylhept-5-en-3-ol C) isopropyl-(4-isopropyl-4-methylbut-2-enyl) ether D) 4 isopropoxy-4,5-dimethylhex-2-ene E) 4-isopropyl-4-methylbut-2-en-isopropyl ether 12. Which of the following...
Oxygen-containing Compounds 1. Which of the following will NOT convert 1-butanol into 1-chlorobutane in one step? a. SOCI2 b. PCl3 c. HCI d. CCl4
14. Which of the following reagents should be used to prepare tert-butyl ethyl ether a) tert-butyl bromide and sodium ethoxide b) tert-butyl alcohol and ethyl bromide c) tert-butyl alcohol and ethanol d) potassium tert-butoxide and ethyl bromide 15. What is the major organic product obtained from the following reaction? A) 1 B) 2 C) 3 D) 4 16. What product is formed when methyloxirane is treated with ethylmannesium bromide followed by treatment with aqueous acid? A) 1-pentanol B) 2-pentanol C)...
please answer the following: 1. Give the reagents for the following reaction sequence: O obco 2. Rank the following compounds in increasing order of reactivity towards nucleophilic acyl substitution (least to most reactive) goblok 3. Give the products for the following reactions: OH 1. KMnO/H* protection H01 pTSA 2. MeMgBr (excess) 3. H30* 2. SOCIzpyr. 1. deprotect. HCI PPh Good Luck Homework 3-Spring 2020 W Downloads/Homework%203-Spring%202020.pdf 4. Give the products for the following reactions: 1. H30+ ethene 2. H.Cro 1....
5) Which of the following compounds is hydrolyzed the slowest in aqueous NaOH? І п ш IV у E) II A) III B) I C) IV 6) 6) What is the major product when (CH3)2CHCH2CH2Br undergoes the following reaction sequence: (Step 1) Mg, ether (Step 2) CO2 (Step 3) H30+ A) 4-methyl-1-pentanol B) 2-methyl-2-butanol C) 4-methylpentanoic acid D) 3-methylbutanoic acid 7) Diisobutylaluminum hydride can be used to carry out which of the following conversions? A) aldehyde to carboxylic acid B)...
2. Which of the following compounds is likely to undergoa gas-evolution reaction in an aqueous solution? H2SO4 CHнCOOн HаСОз HCI HF Use the slider to rate your confidence on this question.
A synthetic trap occurs when a reaction can give more than one desired product. For the reaction below, draw the structures of the two organiccompounds that were actually formed following the addition of \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{Li}\) and subsequent aqueous acid workup.Draw the structures of the two organic compounds which were actually isolated so that all eleven carbons involved in the reactions are accounted for in your answer.
1. In both the sodium iodide test and the silver nitrate test, why does 2-bromobutane react faster than 2-chlorobutane? Bromine is a better leaving group since it is a weaker base than chlorine is. 2. a. Why does benzyl chloride react under both SN1 and SN2 conditions? Benzyl chloride is a primary alkyl halide, hence reactive under SN2 conditions. The primary carbocation formed due to the departure of Cl- is stabilized by the pi electrons in the benzene ring. b. Why is...
Questions 2-10 please!! 1) A substitution reaction is: [2] a) A reaction during which an OH group of a molecule is replaced by a halogen. b) A reaction during which water is the leaving group. c) A reaction during which a functional group of a molecule is replaced by an electrophile. d) A reaction during which a functional group of a molecule is replaced by another functional group. V 12 2) Substitution reactions are classified either as electrophilic or nucleophilic...
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...