Organic Chemistry - Standalone book
10th Edition
ISBN: 9780073511214
Author: Francis A Carey Dr., Robert M. Giuliano
Publisher: McGraw-Hill Education
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Textbook Question
Chapter 11, Problem 47P
Show how to prepare each of the following compounds from propene and any necessaryorganic or inorganic reagents:
a) Allyl bromide
b)
c)
d)
e)
f) Allyl alcohol
g)
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Check out a sample textbook solutionStudents have asked these similar questions
10) For the reaction between isopropyl 1-propyl (or 'n-propyl') ether and HBr, which type of reaction best
matches the expected products?
A) Acid-catalyzed dehydration
B) Nucleophilic substitution reaction
C) Ether cleavage reaction
D) Nucleophilic addition-elimination reaction
The common name for the Following compound 9s:
a) disec -butyl-ether
b) dPbutyl ether
c) 1- Psobutox?do – 2 - methyl propane
d) disopropyl ether
The common name for the followPng compound Ps:
a) butyl methyl ether
b) Pso bu tyl methyl ether
C) methyl sec-butyl ether
d) sec-butyl methyl ether
The IUPAC name is:
HO
a) l,,4-trimethylcyclohexano)
b) I,4,4 - trimethyl cyclohexanol
C) 3,3,6-te?methyl cyclohexano)
d) 2,5,5-trimethylayclohexano)
The IUPAC name 9s:
OH
Br
a) 6-bromo-2-methylcyclohew-1-en-3-01
b) 4 -bromo- a- methylycohen-2-en -\-0l
C) S-bromo -1-methyicgclohex-l- en-2-01
d) 3-bromo-l-methylcyclohex-1-en-6-01
e) s-bromo-2-methylcyclohexol- en -2-01
Chapter 11 Solutions
Organic Chemistry - Standalone book
Ch. 11.1 - Prob. 1PCh. 11.1 - Prob. 2PCh. 11.2 - The two compounds shown differ by a factor of 60...Ch. 11.2 - Prob. 4PCh. 11.2 - Prob. 5PCh. 11.2 - Prob. 6PCh. 11.3 - Prob. 7PCh. 11.3 - Prob. 8PCh. 11.3 - Evaluate 2,3,3-trimethyl-1-butene as a candidate...Ch. 11.4 - After heating a solution of allyl tert-butyl...
Ch. 11.5 - Prob. 11PCh. 11.6 - Prob. 12PCh. 11.8 - Prob. 13PCh. 11.9 - What dienes containing isolated double bonds are...Ch. 11.10 - Prob. 15PCh. 11.10 - Prob. 16PCh. 11.11 - Prob. 17PCh. 11.12 - Dicarbonyl compounds such as quinones are reactive...Ch. 11.12 - 2,3-Di-tert-butyl-1,3-butadiene is extremely...Ch. 11.12 - Methyl acrylate (H2C=CHCO2CH3) reacts with...Ch. 11.13 - Prob. 21PCh. 11.14 - What diene and dienophile could you use to prepare...Ch. 11.14 - Write equations in the synthetic direction for the...Ch. 11.16 - Prob. 24PCh. 11.16 - Prob. 25PCh. 11 - Write structural formulas for each of the...Ch. 11 - Give an acceptable IUPAC name for each of the...Ch. 11 - A certain species of grasshopper secretes an...Ch. 11 - Which of the following are chiral?...Ch. 11 - Describe the molecular geometry expected for...Ch. 11 - Prob. 31PCh. 11 - What compound of molecular formula C6H10 gives...Ch. 11 - Prob. 33PCh. 11 - Prob. 34PCh. 11 - Prob. 35PCh. 11 - Prob. 36PCh. 11 - Identify the more reactive dienophile in each of...Ch. 11 - Prob. 38PCh. 11 - Prob. 39PCh. 11 - Prob. 40PCh. 11 - Prob. 41PCh. 11 - Prob. 42PCh. 11 - Prob. 43PCh. 11 - Prob. 44PCh. 11 - Prob. 45PCh. 11 - Prob. 46PCh. 11 - Show how to prepare each of the following...Ch. 11 - Prob. 48PCh. 11 - Prob. 49PCh. 11 - Prob. 50PCh. 11 - Compound A was converted to compound B by the...Ch. 11 - Suggest reasonable explanations for each of the...Ch. 11 - Prob. 53PCh. 11 - Prob. 54PCh. 11 - Prob. 55DSPCh. 11 - Prob. 56DSPCh. 11 - Prob. 57DSPCh. 11 - Prob. 58DSPCh. 11 - Prob. 59DSP
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- What is the major product of the reaction of 2-hexyne with excess bromine? A) 2-bromohexene B) 2,3-dibromohexene C) 2-bromohexane D) 2,3-dibromohexane E) 2,2,3,3-tetrabromohexanearrow_forwardWrite the chemical equation showing reactants, products and catalysts needed (if any) for thefollowing reactions. Write the IUPAC name of the product right beside the structure. a) Reaction of two phenol b) Reaction of 2-bromophenol with sodium hydroxide c) Reaction of potassium phenoxide with 2-chloropentane d) Reaction of isopropyl propyl ether with HBr e) Reaction of 3-methylpentan-3-ol with sulfuric acid f) Dehydration of 1,5-hepta-diolg) Oxidation of 1-decanolh) Hydration od hepta-2,3-dienearrow_forwardFor each of the following compounds, draw its structure. a) 2,4,6-trimethyl-3-nonanone b) trans-2-tert-butylcyclohexanol c) sec.-butyl propyl ether gamma-bromo-beta-methoxybutyraldehyde d) e) 3,3-diethyl-2-hexanethiolarrow_forward
- 1. Write in the correct reagents to accomplish these reactions. a) 2-methylcyclohexanol b) benzyl alcohol → 1-bromo-2-methylcyclohexane benzaldehydearrow_forwardSynthesize 4-octanol using only 1-butene as your source of carbonarrow_forward1. Write in the correct reagents to accomplish these reactions. a) 2-methyl-2-pentanol b) CH3CH2CH₂OH → 2-chloro-2-methylpentane CH3CH₂CHarrow_forward
- 18. Draw the structure of the following compounds. a) 2-fiJoro-2,3-dimethy!butane b) 2-bromo-1-chloro-3-iodopropane c) (2-bromoethyl)cyclobutanearrow_forwardWrite an equation for each of the following two-step reactions: - cyclohexanone a) Cyclohexene to b) 1-bromobutane to butanalarrow_forwardProvide the major organic product of the following reaction. but-1-yne 1) Sia₂BH 2) H₂O₂, OH What is it called when an enol converts to a keto? A) Keto-enol isomerism B) Keto-enol tater tot-ism C) Keto-enol conversion D) Keto-enol tautomerismarrow_forward
- Write in the correct reagents for these transformations: a) cyclohexanol -→ chlorocyclohexane b) 2-butanone 2-butanol ward 2-butanol 2-butanone toluene - → benzoic acid nitrobenzene → anilinearrow_forwardThe ACS exam at the end of this semester covers a limited amount of IUPAC nomenclature mostly from Organic I. An example is given below, what is the IUPAC name of of the compound whose structure is shown in the box? A) E-1- butylidene-1-iodo-propane B) E-5-iodo-4-heptene C) E-1-(1-iodopropylidene)-butane D) E-3-iodo-3-heptene A Вarrow_forwardDraw the structures of the following aldehydes / ketones: 1.) 3-chloro-3-methylhexanal 2.) 3,4-diethyl-3-methylhexan-2-one 3.) 5-bromo-3-methyheptanalarrow_forward
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How to Design a Total Synthesis; Author: Chemistry Unleashed;https://www.youtube.com/watch?v=9jRfAJJO7mM;License: Standard YouTube License, CC-BY