EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
9th Edition
ISBN: 9780136781776
Author: Wade
Publisher: PEARSON CO
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Textbook Question
Chapter 15, Problem 15.26SP
Show how the reaction of an allylic halide with a Grignard reagent might be used to synthesize the following hydrocarbons.
- a. 5-methylhex-1-ene
- b. 2,5,5-trimethylhept-2-ene
- c. 1-cyclopentylpent-2-ene
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Students have asked these similar questions
1) Which of the following the alkyl halides reacts the fastest in an SN2 reaction? *
A. 1-Chloropropane
B. 1-Bromopropane
C. 1-Fluoropropane
D. 1-Iodopropane
E. Alkyl halides do not undergo SN2 reactions
2) The IUPAC name of the expected Markovnikov addition product of HI to 2-methyl-2-butene is __________.
Name the following
compound according to the
IUPAC method.
CH3
CH2=CH-C- CH–CH3
Br OH
A. 3-bromo-3-methyl-2-hydroxypent-
4-ene
B. 5-formyl-1,3-dibromobenzene
C. 3-bromo-3-methylpent-4-en-2-ol
D. 3-bromo-3-methylpent-2-en-4-ol
A hydrocarbon, C6H12, on ozonolysis gives only one product which does not give silver mirror with Tollens' reagent. The hydrocarbon is ______________.
a. 3-Hexene
b. 2-Hexene
c. 2-Methyl-2-pentene
d. 2,3-Dimethyl-2-butene
Chapter 15 Solutions
EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
Ch. 15.2 - Prob. 15.1PCh. 15.2 - Prob. 15.2PCh. 15.2 - Prob. 15.3PCh. 15.4 - Prob. 15.4PCh. 15.4 - Prob. 15.5PCh. 15.5 - Treatment of an alkyl halide with AgNO3 in alcohol...Ch. 15.5 - Propose a mechanism for each reaction, showing...Ch. 15.6 - When Br2 is added to buta-1,3-diene at 15 C, the...Ch. 15.7 - Prob. 15.9PCh. 15.7 - When N-bromosuccinimide is added to hex-1-ene in...
Ch. 15.7 - Prob. 15.11PCh. 15.9 - Addition of 1-bromobut-2-ene to magnesium metal in...Ch. 15.10 - Show how you might synthesize the following...Ch. 15.11 - Predict the products of the following proposed...Ch. 15.11 - Prob. 15.15PCh. 15.11A - Prob. 15.16PCh. 15.11B - Prob. 15.17PCh. 15.11B - Predict the products of the following Diels-Alder...Ch. 15.12C - Prob. 15.19PCh. 15.12C - Prob. 15.20PCh. 15.13C - Prob. 15.21PCh. 15.13D - Using the examples in Table15-2 to guide you,...Ch. 15.14 - Phenolphthalein is an acid-base indicator that is...Ch. 15 - Prob. 15.24SPCh. 15 - Prob. 15.25SPCh. 15 - Show how the reaction of an allylic halide with a...Ch. 15 - Prob. 15.27SPCh. 15 - A solution was prepared using 0.0010 g of an...Ch. 15 - Prob. 15.29SPCh. 15 - Prob. 15.30SPCh. 15 - Prob. 15.31SPCh. 15 - Prob. 15.32SPCh. 15 - Prob. 15.33SPCh. 15 - Give the structures of the products represented by...Ch. 15 - Furan and malemide undergo a Diels-Alder reaction...Ch. 15 - Prob. 15.36SPCh. 15 - Prob. 15.37SPCh. 15 - Prob. 15.38SPCh. 15 - Prob. 15.39SPCh. 15 - Determine whether each structure is likely to be...Ch. 15 - An important variation of the Diels-Alder reaction...
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- Show how to convert propene to each of these compounds, using any inorganic reagents as necessary. a. Propane b.1,2-Propanediol c. 1-Propanol d. 2-Propanol e. Propanal f. Propanone g. Propanoic acid h. l-Bromo-2-propanol i. 3-Chloropropene j. 1,2,3-Trichloropropane k. 1-Chloropropane l. 2-Chloropropane m. 2-Propen-1-ol n. Propenalarrow_forwardWhat substitution products are obtained when each of the following compounds is added to a solution of sodium acetate in acetic acid? a. 2-chloro-2-methyl-3-hexene b. 3-bromo-1-methylcyclohexenearrow_forwardUsing the E/Z naming system - What is the product from reacting 3-octyne with hydrogen gas and Lindlar's catalyst (also known as "poisoned Pd")? A. Z-3-octene B. E-3-octene C. E-2-octene D. 2E,4E-octadienearrow_forward
- 1. Which will be the major product if 3,3-demethyl-2- butanol to react in 85% of H3PO4? a. 2,3-demethyl-1-butene b. 2,3-demethyl-2-butene c. 2,2-demethyl-2-butene d. 3,3-demethyl-2-butenearrow_forwardConsider 3-methylpent-2-ene, if it undergoes hydroboration, which of the following final product is formed? a. 3-methylpent-2-en-2-ol b. 3-methylpentan-3-ol c. 3-methylpentan-2-ol d. 2-methylpentan-3-olarrow_forwardFor each reaction identify the reaction type. Reaction Туре a. Methylbenzene and bromine in the presence of ultraviolet light forming 1- bromo-2-methylbenzene and hydrogen bromide. b. 2-methyldecane plus hydrogen reacts to produce heptane and butane c. Hex-2-ene plus hydrogen chloride produces 2-chlorohexane. d. Propane plus pentane reacts to produce 1,2-dimethylcyclohexane and hydrogenarrow_forward
- Draw the principal neutral organic product formed by the reaction of 2.3-dimethyl-1,3-butadiene with the given reagents. a. Excess H2 and Platinum catalyst b. 1 mole HCl (product of 1,2-addition) c. 1 mole HCl (product of 1,4-addition)arrow_forward2-Methyl-2-butene reacts with HBr in the presence of peroxide to give a. a secondary alkyl bromide. b. a primary alkyl bromide. c. a tertiary alkyl bromide. d. a vicinal dibromide.arrow_forwardDraw the product or products that will be obtained from the reaction of cis-2-butene and trans-2-butene with each of the following reagents. If a product can exist as stereoisomers, show which stereoisomers are formed. 1. HCl. 4.Br2 in CH2Cl2 7. H2O + H2SO4 2. BH3/THF, followed by HO-, H2O2, H2O 5. Br2 + H2O 8. CH3OH + H2SO4 3. a peroxyacid 6. H2 + Pd/Carrow_forward
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