ORGANIC CHEMISTRY SMARTWORK5 - ACCESS
2nd Edition
ISBN: 9780393432534
Author: KARTY
Publisher: NORTON
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Question
Chapter 16, Problem 16.31YT
Interpretation Introduction
Interpretation:
Hexane has six carbon atoms and dodecane has
Concept introduction:
The total number of carbon atoms in a molecule can be computed from the intensity of the
The equation
The base peak is the peak with the greatest intensity (usually set to
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Students have asked these similar questions
Name the alkyl group as if the dashed line were where it was connect to the rest of the molecule, state whether it is primary, secondary, or tertiary.
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View the first compound name provided in Table 6. Follow the steps below and draw each part of the structure on a piece of paper.
Determine the number of carbons present in the compound based on the base name.
Draw the carbon chain and include any double or triple bonds if indicated in the suffix of the base name.
Number each carbon. The carbons can be numbered from left to right or right to left.
Draw any substituents on the corresponding carbon atom for which is indicated in the name. Refer to Figures 3 and 4 in the background for a visual representation of numbered carbons with corresponding substituents.
Check that each carbon atom has a total of 4 bonds.
Chapter 16 Solutions
ORGANIC CHEMISTRY SMARTWORK5 - ACCESS
Ch. 16 - Prob. 16.1PCh. 16 - Prob. 16.2PCh. 16 - Prob. 16.3PCh. 16 - Prob. 16.4PCh. 16 - Prob. 16.5PCh. 16 - Prob. 16.6PCh. 16 - Prob. 16.7PCh. 16 - Prob. 16.8PCh. 16 - Prob. 16.9PCh. 16 - Prob. 16.10P
Ch. 16 - Prob. 16.11PCh. 16 - Prob. 16.12PCh. 16 - Prob. 16.13PCh. 16 - Prob. 16.14PCh. 16 - Prob. 16.15PCh. 16 - Prob. 16.16PCh. 16 - Prob. 16.17PCh. 16 - Prob. 16.18PCh. 16 - Prob. 16.19PCh. 16 - Prob. 16.20PCh. 16 - Prob. 16.21PCh. 16 - Prob. 16.22PCh. 16 - Prob. 16.23PCh. 16 - Prob. 16.24PCh. 16 - Prob. 16.25PCh. 16 - Prob. 16.26PCh. 16 - Prob. 16.27PCh. 16 - Prob. 16.28PCh. 16 - Prob. 16.29PCh. 16 - Prob. 16.30PCh. 16 - Prob. 16.31PCh. 16 - Prob. 16.32PCh. 16 - Prob. 16.33PCh. 16 - Prob. 16.34PCh. 16 - Prob. 16.35PCh. 16 - Prob. 16.36PCh. 16 - Prob. 16.37PCh. 16 - Prob. 16.38PCh. 16 - Prob. 16.39PCh. 16 - Prob. 16.40PCh. 16 - Prob. 16.41PCh. 16 - Prob. 16.42PCh. 16 - Prob. 16.43PCh. 16 - Prob. 16.44PCh. 16 - Prob. 16.45PCh. 16 - Prob. 16.46PCh. 16 - Prob. 16.47PCh. 16 - Prob. 16.48PCh. 16 - Prob. 16.49PCh. 16 - Prob. 16.50PCh. 16 - Prob. 16.51PCh. 16 - Prob. 16.52PCh. 16 - Prob. 16.53PCh. 16 - Prob. 16.54PCh. 16 - Prob. 16.55PCh. 16 - Prob. 16.56PCh. 16 - Prob. 16.57PCh. 16 - Prob. 16.58PCh. 16 - Prob. 16.59PCh. 16 - Prob. 16.60PCh. 16 - Prob. 16.61PCh. 16 - Prob. 16.62PCh. 16 - Prob. 16.63PCh. 16 - Prob. 16.64PCh. 16 - Prob. 16.65PCh. 16 - Prob. 16.66PCh. 16 - Prob. 16.67PCh. 16 - Prob. 16.68PCh. 16 - Prob. 16.69PCh. 16 - Prob. 16.70PCh. 16 - Prob. 16.71PCh. 16 - Prob. 16.72PCh. 16 - Prob. 16.73PCh. 16 - Prob. 16.74PCh. 16 - Prob. 16.75PCh. 16 - Prob. 16.76PCh. 16 - Prob. 16.77PCh. 16 - Prob. 16.78PCh. 16 - Prob. 16.79PCh. 16 - Prob. 16.80PCh. 16 - Prob. 16.81PCh. 16 - Prob. 16.82PCh. 16 - Prob. 16.83PCh. 16 - Prob. 16.84PCh. 16 - Prob. 16.85PCh. 16 - Prob. 16.86PCh. 16 - Prob. 16.87PCh. 16 - Prob. 16.88PCh. 16 - Prob. 16.89PCh. 16 - Prob. 16.1YTCh. 16 - Prob. 16.2YTCh. 16 - Prob. 16.3YTCh. 16 - Prob. 16.4YTCh. 16 - Prob. 16.5YTCh. 16 - Prob. 16.6YTCh. 16 - Prob. 16.7YTCh. 16 - Prob. 16.8YTCh. 16 - Prob. 16.9YTCh. 16 - Prob. 16.10YTCh. 16 - Prob. 16.11YTCh. 16 - Prob. 16.12YTCh. 16 - Prob. 16.13YTCh. 16 - Prob. 16.14YTCh. 16 - Prob. 16.15YTCh. 16 - Prob. 16.16YTCh. 16 - Prob. 16.17YTCh. 16 - Prob. 16.18YTCh. 16 - Prob. 16.19YTCh. 16 - Prob. 16.20YTCh. 16 - Prob. 16.21YTCh. 16 - Prob. 16.22YTCh. 16 - Prob. 16.23YTCh. 16 - Prob. 16.24YTCh. 16 - Prob. 16.25YTCh. 16 - Prob. 16.26YTCh. 16 - Prob. 16.27YTCh. 16 - Prob. 16.28YTCh. 16 - Prob. 16.29YTCh. 16 - Prob. 16.30YTCh. 16 - Prob. 16.31YTCh. 16 - Prob. 16.32YTCh. 16 - Prob. 16.33YTCh. 16 - Prob. 16.34YT
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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 IUPAC name of the compound shown here? (view attatchement) **FIRST TIME YOU ANSWERE THIS WAS WRONG, please help with correct answer. The answer you gave me before was 1,4-dimethylcyclobut-1-ene but is was WRONG . This is what the paragraph also said next to the question "Alkanes are called saturated hydrocarbons because each carbon atom has the maximum number of hydrogen atoms. In contrast, alkenes and alkynes are unsaturated because they contain double or triple bonds that reduce the number of hydrogen atoms in the compound. When naming unsaturated hydrocarbons, a suffix reflects the type of multiple bond in the compound: ene is used for alkenes (double bond), and yne is used for alkynes (triple bond). For cyclic alkenes and alkynes, the ring is numbered such that the double or triple bond is between the first two carbon atoms. For straight-chain molecules, the numbering starts at one end of the chain, so the location of the double or triple bond must be…arrow_forwardPart A Alkanes are molecules that contain only carbon and hydrogen and have only single bonds. Straight-chain What is the molecular formula for the alkane shown in the model? alkanes have all the carbon atoms connected in a Express your answer as a chemical formula. row, branched-chain alkanes have branching connections of carbon atoms, and cycloalkanes contain rings of carbon atoms. • View Available Hint(s) ? CH, CH, DA chemical reaction does not occur for this question. Submit Previous Answers X Incorrect; Try Again; 5 attempts remaining Figure View Available Hint(s) Pentanearrow_forwardNow, if you take the above compound, and place a METHYL group on the carbon in the BACK LEFT position of the ring, you will have a cycloalkane with three groups, all on different neighboring carbons. The correct complete IUPAC name for this NEW compound would bearrow_forward
- What two tests can be used to test for the presence of a double or triple bond (i.e., will result in a positive test while an alkane will have a negative result)? List what physical observations you expect to see for each type of compound.arrow_forwardthe question below is from Organic Chemistry and deals with Substitution RXNarrow_forwardExamine the cycloalkane above. There are two carbons that make up the front of the ring, and three carbons that make up the back of the ring. Now, if you take the above compound, and place a METHYL group on the carbon in the frontmost right position of the ring, you will have a cycloalkane with three groups, all on different neighboring carbons. The correct complete IUPAC name for this NEW compound would be (including numbers when required): cyclopentanearrow_forward
- Answer 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_forwardThe instructions are to 1. list the functional group that differentiates benzhydrol from biphenyl 2. List the class of organic compound that differentiates benzhydrol from biphenyl. Would the answer for functional group be hydroxyl? I'm not sure about the class..?arrow_forwardIf methyl substituents are present in the 3rd and 4th Carbon, which among what will be the name of the molecule ?arrow_forward
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