Concept explainers
(a)
Interpretation:
Double bond in the in the cyclohexene has to be labeled.
Concept Introduction:
Cis isomer: When the two
Trans isomer: When the two functional groups are present on the opposite side of the double bond, then the compound is said to be as trans isomer.
(b)
Interpretation:
Double bond in the in the cyclodeca-1,4-diene has to be labeled.
Concept Introduction:
Cis isomer: When the two functional groups are present on the same side of the double bond, then the compound is said to be as cis isomer.
Trans isomer: When the two functional groups are present on the opposite side of the double bond, then the compound is said to be as trans isomer.
Want to see the full answer?
Check out a sample textbook solutionChapter 11 Solutions
Connect 1-Semester Online Access for Principles of General, Organic & Biochemistry
- Determine which cyclohexane structure has the MOST energy (is the LEAST stable)?arrow_forwardWhich of the following statements about cyclooctatetraene (the Lewis structure of which could be represented by an 8-membered ring with 4 conjugated pi bonds) is false?arrow_forward(c) There is one (1) other positional isomer of X missing for reaction II. Draw the structural formula of this isomer.arrow_forward
- Which is an isomer to octane?arrow_forwardAnswer this question:How to draw the line bond formula or lewis structure of a methyl ketone with the chemical formula C6H5C3H5O? (also taking into consideration the solubility test and chemical test results provided below) Based on the results of the solubility tests the compound is insoluble in water, 10% NaOH and 10% HCl but soluble in concentrated H2SO4. The functional group/class is identified to be Methyl Ketone, based on the results of the chemical tests on Table 2. CHEMICAL TEST OBSERVATIONS +(compound tested positive for the chemical reaction)/ otherwise (-) Molisch test turbid colorless solution - 2,4-DNP test formation of orange-yellow precipitates + Tollen’s test turbid colorless solution - Ninhydrin test clear pale-yellow solution - iodoform test clear pale-yellow solution +arrow_forwardb) C8H13Bг2Cl2O2 Isomer #1: Name of Isomer #1: Name of Isomer #2: Name of Isomer #3: Isomer #2: Isomer #3:arrow_forward
- How would you best describe the C-C bonds lengths in benzene relative to cyclohexane? Hypothesize why these results are observed.arrow_forwardRank the C–H bonds in acetylene, ethylene and ethane in order of strength.arrow_forwardWhen cyclopropane is treated with HI, 1-idopropane is formed. A similar type of reaction does not occur with cyclopentene or Cyclohexane. Suggest an explanation for cyclopropane’s reactivity.arrow_forward
- O O O O O Classify the pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric. Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each. Br Br CH H3C Br Br Br Br Compound 1 Compound 2 The compounds are enantiomers not isomeric O constitutional isomers O identical diastereomers The correct IUPAC names are:arrow_forwardWrite down the general formula for an alkyne (Using Cn and H). Explain how the ratio between C and H in C3H4 meets the general rule criteria to be an alkyne. please explain completelyarrow_forwardDo the CC bond lengths in benzene alternate short-long-short-long around the ring? Why or why not?arrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub CoChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning