
EBK FUNDAMENTALS OF GENERAL, ORGANIC, A
8th Edition
ISBN: 8220102895805
Author: Peterson
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 13, Problem 13.36AP
(a)
Interpretation Introduction
Interpretation:
The IUPAC name of the given structure to be predicted
Concept Introduction:
- Name the parent compound: Find the longest chain containing the double bond or triple bond and add the suffix ‘-ene’ for
alkene or ‘-yne’ foralkyne to the end of the main chain name. - Number the carbon atoms in the main chain so that those with multiple bonds have the lowest index numbers possible:
- Write the full name: List the substituents in alphabetical order. Use commas to separate the numbers and the hyphen to separate number from words. Indicate the position of double or triple bond in chain by giving the number of the first multiple-bond carbon.
(b)
Interpretation Introduction
Interpretation:
The IUPAC name of the given compound to be predicted
Concept Introduction:
IUPAC naming nomenclature:
- Name the parent compound: Find the longest chain containing the double bond or triple bond and add the suffix ‘-ene’ for alkene or ‘-yne’ for alkyne to the end of the main chain name.
- Number the carbon atoms in the main chain so that those with multiple bonds have the lowest index numbers possible:
- Write the full name: List the substituents in alphabetical order. Use commas to separate the numbers and the hyphen to separate number from words. Indicate the position of double or triple bond in chain by giving the number of the first multiple-bond carbon.
(c)
Interpretation Introduction
Interpretation:
The IUPAC name of the given compound to be predicted
Concept Introduction:
IUPAC naming nomenclature:
- Name the parent compound: Find the longest chain containing the double bond or triple bond and add the suffix ‘-ene’ with the parent for alkene or ‘-yne’ with the parent for alkyne to the end of the main chain name.
- Number the carbon atoms in the main chain so that those with multiple bonds have the lowest index numbers possible:
- Write the full name: List the substituents in alphabetical order. Use commas to separate the numbers and the hyphen to separate number from words. Indicate the position of double or triple bond in chain by giving the number of the first multiple-bond carbon.
(d)
Interpretation Introduction
Interpretation:
The IUPAC name of the given compound to be predicted
Concept Introduction:
IUPAC naming nomenclature:
- Name the parent compound: Find the longest chain containing the double bond or triple bond and add the suffix ‘-ene’ for alkene or ‘-yne’ for alkyne to the end of the main chain name.
- Number the carbon atoms in the main chain so that those with multiple bonds have the lowest index numbers possible:
- Write the full name: List the substituents in alphabetical order. Use commas to separate the numbers and the hyphen to separate number from words. Indicate the position of double or triple bond in chain by giving the number of the first multiple-bond carbon.
(e)
Interpretation Introduction
Interpretation:
The IUPAC name of the given compound to be predicted
Concept Introduction:
IUPAC naming nomenclature:
- Name the parent compound: Find the longest chain containing the double bond or triple bond and add the suffix ‘-ene’ for alkene or ‘-yne’ for alkyne to the end of the main chain name.
- Number the carbon atoms in the main chain so that those with multiple bonds have the lowest index numbers possible:
- Write the full name: List the substituents in alphabetical order. Use commas to separate the numbers and the hyphen to separate number from words. Indicate the position of double or triple bond in chain by giving the number of the first multiple-bond carbon.
(d)
Interpretation Introduction
Interpretation:
The IUPAC name of the given compound to be predicted
Concept Introduction:
IUPAC naming nomenclature:
- Name the parent compound: Find the longest chain containing the double bond or triple bond and add the suffix ‘-ene’ for alkene or ‘-yne’ for alkyne to the end of the main chain name.
- Number the carbon atoms in the main chain so that those with multiple bonds have the lowest index numbers possible:
- Write the full name: List the substituents in alphabetical order. Use commas to separate the numbers and the hyphen to separate number from words. Indicate the position of double or triple bond in chain by giving the number of the first multiple-bond carbon.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Can koch's postulates of disease causation be applied to non-microorganism disease pathogens (such as molecules)?
Here is my literature Beta Carotene HPLC analysis graph.
Can you help me explain what each peak is at each retention time?
Thank You :D
I have a literature B-Carotene HPLC graph in which showcases a retention time of roughly 23.6 and 25.1.
Please help me compare my two different Anti-Oxidant Juice graphs. (Attached)
The juices provided are: V8 Carrot Ginger Blend and V8 Original Blend
Noticing the HPLC graphs I saw no peaks for the Original Blend for B-Carotene.
However the Carrot Ginger Blend showed similar peaks --> Why is this reason?
Please explain in terms of Retention time and Area (Under Curve).
Thank You!
Chapter 13 Solutions
EBK FUNDAMENTALS OF GENERAL, ORGANIC, A
Ch. 13.2 - Prob. 13.1PCh. 13.2 - Prob. 13.2PCh. 13.2 - What are the IUPAC names of the two alkenes shown...Ch. 13.3 - Prob. 13.4PCh. 13.3 - Prob. 13.5PCh. 13.3 - Prob. 13.6KCPCh. 13.5 - Prob. 13.7PCh. 13.5 - Many biological transformations can be simply...Ch. 13.5 - (a) After the reaction of 11-cis-retinal with...Ch. 13.5 - Prob. 13.2CIAP
Ch. 13.5 - Prob. 13.3CIAPCh. 13.6 - Prob. 13.9PCh. 13.6 - Prob. 13.10PCh. 13.6 - Prob. 13.11PCh. 13.6 - Prob. 13.12PCh. 13.6 - Prob. 13.13PCh. 13.6 - Prob. 13.14KCPCh. 13.6 - Prob. 13.1MRPCh. 13.6 - Prob. 13.2MRPCh. 13.6 - Prob. 13.3MRPCh. 13.7 - Prob. 13.15PCh. 13.7 - Prob. 13.16PCh. 13.8 - Prob. 13.17PCh. 13.8 - Polychlorotrifluoroethylene (PCTFE (Kel-F)) is a...Ch. 13.9 - Prob. 13.19PCh. 13.9 - Prob. 13.20PCh. 13.9 - Prob. 13.21KCPCh. 13.10 - What products will be formed when toluene is...Ch. 13.10 - Prob. 13.23PCh. 13.10 - Prob. 13.4CIAPCh. 13.10 - Prob. 13.5CIAPCh. 13.10 - Prob. 13.6CIAPCh. 13 - Prob. 13.24UKCCh. 13 - Prob. 13.25UKCCh. 13 - Prob. 13.26UKCCh. 13 - Draw the product from reaction of the following...Ch. 13 - Prob. 13.28UKCCh. 13 - Prob. 13.29UKCCh. 13 - Prob. 13.30APCh. 13 - Prob. 13.31APCh. 13 - What family-name endings are used for alkenes,...Ch. 13 - Prob. 13.33APCh. 13 - Prob. 13.34APCh. 13 - Write structural formulas for compounds that meet...Ch. 13 - Prob. 13.36APCh. 13 - Prob. 13.37APCh. 13 - Draw structures corresponding to the following...Ch. 13 - Draw structures corresponding to the following...Ch. 13 - Seven alkynes have the formula C6H10. Draw them,...Ch. 13 - Prob. 13.41APCh. 13 - Prob. 13.42APCh. 13 - There are four different pentenes having the...Ch. 13 - Prob. 13.44APCh. 13 - Prob. 13.45APCh. 13 - Draw line structures for the following alkenes....Ch. 13 - Which compound(s) in Problem 13.43 can exist as...Ch. 13 - Prob. 13.48APCh. 13 - Prob. 13.49APCh. 13 - Which of the following pairs are isomers, and...Ch. 13 - Prob. 13.51APCh. 13 - Prob. 13.52APCh. 13 - Prob. 13.53APCh. 13 - Prob. 13.54APCh. 13 - Prob. 13.55APCh. 13 - Prob. 13.56APCh. 13 - Prob. 13.57APCh. 13 - Prob. 13.58APCh. 13 - Prob. 13.59APCh. 13 - What alkene could you use to make the following...Ch. 13 - Prob. 13.61APCh. 13 - Prob. 13.62APCh. 13 - Prob. 13.63APCh. 13 - Prob. 13.64APCh. 13 - For each of the following reagents, decide whether...Ch. 13 - Prob. 13.66APCh. 13 - Prob. 13.67APCh. 13 - Prob. 13.68APCh. 13 - Salicylic acid (o-hydroxybenzoic acid) is used as...Ch. 13 - The following names are incorrect by IUPAC rules....Ch. 13 - Prob. 13.71CPCh. 13 - Prob. 13.72CPCh. 13 - Prob. 13.73CPCh. 13 - Prob. 13.74CPCh. 13 - Menthene, a compound found in mint plants, has the...Ch. 13 - Prob. 13.76CPCh. 13 - Prob. 13.77CPCh. 13 - Two products are possible when 2-pentene is...Ch. 13 - Ocimene, a compound isolated from the herb basil,...Ch. 13 - Describe how you could prepare the following...Ch. 13 - Which of the following compounds are capable of...Ch. 13 - Prob. 13.82GPCh. 13 - Superglue is an alkene polymer made from the...Ch. 13 - Draw all possible C5H10 alkene isomers having a...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biochemistry and related others by exploring similar questions and additional content below.Similar questions
- Calculate pH of a solution prepared by dissolving 1.60g of sodium acetate, in 88.5 mL of 0.10 M acetic acid. Assume the volume change upon dissolving the sodium acetate is negligible. Ka is 1.75 x 10^-5arrow_forwardShow a mechanism that leads to the opening of the ring below under acid-catalyzed conditions. Give the correct Fischer projection for this sugar.arrow_forwardWhat is the stereochemical relationship between B & C?arrow_forward
- Don't use ai or any chat gpt will dislike okk just use accurate information okkk okkk just solve full accurate. don't use guidelines okk just did it accurate 100% sure experts solve it correct complete solutions okkk follow all instructions requirements okkkarrow_forwardhow would you make this plot in excel?arrow_forwardwhat is the productarrow_forward
- Balance the following equation and list of coefficients in order from left to right. SF4+H2O+—-> H2SO3+HFarrow_forwardProblem 15 of 15 Submit Using the following reaction data points, construct Lineweaver-Burk plots for an enzyme with and without an inhibitor by dragging the points to their relevant coordinates on the graph and drawing a line of best fit. Using the information from this plot, determine the type of inhibitor present. 1 mM-1 1 s mM -1 [S]' V' with 10 μg per 20 54 10 36 20 5 27 2.5 23 1.25 20 Answer: |||arrow_forward12:33 CO Problem 4 of 15 4G 54% Done On the following Lineweaver-Burk -1 plot, identify the by dragging the Km point to the appropriate value. 1/V 40 35- 30- 25 20 15 10- T Км -15 10 -5 0 5 ||| 10 15 №20 25 25 30 1/[S] Г powered by desmosarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Principles Of Radiographic Imaging: An Art And A ...Health & NutritionISBN:9781337711067Author:Richard R. Carlton, Arlene M. Adler, Vesna BalacPublisher:Cengage Learning
- Anatomy & PhysiologyBiologyISBN:9781938168130Author:Kelly A. Young, James A. Wise, Peter DeSaix, Dean H. Kruse, Brandon Poe, Eddie Johnson, Jody E. Johnson, Oksana Korol, J. Gordon Betts, Mark WomblePublisher:OpenStax College

Principles Of Radiographic Imaging: An Art And A ...
Health & Nutrition
ISBN:9781337711067
Author:Richard R. Carlton, Arlene M. Adler, Vesna Balac
Publisher:Cengage Learning

Anatomy & Physiology
Biology
ISBN:9781938168130
Author:Kelly A. Young, James A. Wise, Peter DeSaix, Dean H. Kruse, Brandon Poe, Eddie Johnson, Jody E. Johnson, Oksana Korol, J. Gordon Betts, Mark Womble
Publisher:OpenStax College