ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<
10th Edition
ISBN: 9781259972348
Author: Carey
Publisher: MCG CUSTOM
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Textbook Question
Chapter 10.4, Problem 8P
How many constitutionally isomeric monochlorination products are possible from each of the following?
a)
b)
c)
d)
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find out correct and incorrect IUPAC name and give reason behind it!
8. The following compounds are named incorrectly according to IUPAC rules. Draw out the condensed structural
formula for each compound and name it correctly.
a) 2-propyl-3-butanol
b) 2,5-diethyl-1-pentanone
c) 3,3-dimethyl-1-propanal
d) 1-ethyl-3-cyclohexanol
2-methylhexanoic acid can be synthesized by oxidation of which of the following compounds?
A) 2-methylhexane
B) 2-methyl-1-hexanol
C) 2-methyl-1-hexene
D) 2-methyl-1-hexyne
E) 2-methyl-2-hexanone
Chapter 10 Solutions
ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<
Ch. 10.1 - Prob. 1PCh. 10.1 - Prob. 2PCh. 10.2 - Use the data in Table 10.1 to calculate H for the...Ch. 10.3 - Prob. 4PCh. 10.4 - Prob. 5PCh. 10.4 - Prob. 6PCh. 10.4 - Do the arithmetic involved in converting the...Ch. 10.4 - How many constitutionally isomeric...Ch. 10.4 - Prob. 9PCh. 10.5 - Prob. 10P
Ch. 10.5 - Prob. 11PCh. 10.5 - Prob. 12PCh. 10.6 - Prob. 13PCh. 10.7 - Prob. 14PCh. 10.8 - Prob. 15PCh. 10 - Carboncarbon bond dissociation enthalpies have...Ch. 10 - Use the bond dissociation enthalpy data in Table...Ch. 10 - Use the bond dissociation enthalpy data in Table...Ch. 10 - Write the structure of the major organic product...Ch. 10 - Excluding enantiomers, free-radical chlorination...Ch. 10 - Prob. 21PCh. 10 - Prob. 22PCh. 10 - Prob. 23PCh. 10 - Prob. 24PCh. 10 - Compound A (C6H14) gives three different...Ch. 10 - Prob. 26PCh. 10 - Prob. 27PCh. 10 - Prob. 28PCh. 10 - Prob. 29PCh. 10 - Guiding your reasoning by retrosynthetic analysis,...Ch. 10 - (Z)-9-tricosene [(Z)-CH3(CH2)7CH=CH(CH2)12CH3] is...Ch. 10 - Prob. 32PCh. 10 - Prob. 33PCh. 10 - Prob. 34DSPCh. 10 - Prob. 35DSPCh. 10 - Prob. 36DSPCh. 10 - Prob. 37DSPCh. 10 - Prob. 38DSP
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- Use the IUPAC rules to draw the structures of the following compounds below. Condensed Line-Angle Formula Name of Aldehyde / Structural Molecular Formula Ketone Formula Formula 1) 3-methylcyclohexan-1-one 2) 5-chloroheptan-3-one 3) 4-hydroxybutanal 4) hexan-3,5-dienalarrow_forwardWhich one of the following compounds does not have a secondary carbon? cydopentane butane 2-mathylbutane propane ethyl chloride C Which one of the following compounds does not have hydrogen bonding? triethylamine ethanol water diethylamine methanol A C What is the correct IUPAC name of the following compound? 3,3-dibromo-2-sec-butoxy-5-chloro-4ethylhexane B) 4,4 dibromo-2-chloro-3-ethyl-5-isobutaxcyhexane Br Br C) 3,3-dibromo-4-(chloroethyl)-2-isobutoxyhexane D) 4,4-dibromo-5-sec-butoxy-2-chloro-3-ethylhexane E) 3,3-dibromo-5-chloro-4-ethyl-2-isobutoxyhexane Rank the following compounds accordingly: " What is the correct order of decreasing ACIDITY of the following compounds? ( -- FCHCHNH HI ICHŁCOH на E strongest>_ >_>_>_weakest -What is the correct order of decreasing BASICITY of the following compounds?; CHSO,Na NaCl CH,CH,NHNa C CHONA CH0O,Na strongest >_>_>_>_weakestarrow_forwardProvide the IUPAC name for this compound.arrow_forward
- 1. Write in the correct reagents to accomplish these reactions. a) 2-methyl-2-pentanol b) CH3CH2CH₂OH → 2-chloro-2-methylpentane CH3CH₂CHarrow_forwardAlcohols are really useful starting materials for chemical reactions, as they can be converted into many different organic compounds. For each of the following compounds tell me which alcohol you would need to use. The reaction I have in mind is a single reaction, not a multi step reaction process. Write out the name of the starting alcohol using proper IUPAC rules for naming. A) dipropyl ether B) cyclohexene C) 2,3-dinethylbutanal D) 2,2,4-trimethyl-3-hexanonearrow_forwardGive the IUPAC name for the chemical in the attached image. [click on attachment to view image if you don't see it] CH3CH₂CH₂CH₂CHCH₂CH₂CH₂CH3 CH3CH₂CH₂ O A. 2,2,5,6-tetraethylhexane B. 2,2,5-triethyloctane O C. 3,6-diethyl-3-methylnonane CH₂CH3 D. 3-ethyl-3-methyl-6-propyldecane CH3arrow_forward
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