ORG CHEM CONNECT CARD
6th Edition
ISBN: 9781264860746
Author: SMITH
Publisher: MCG
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 13, Problem 28P
Interpretation Introduction
Interpretation: The resonance structure of the radical that results from the abstraction of a hydrogen atom from the antioxidant BHA is to be drawn.
Concept introduction: Most of the organic structures cannot be represented using single Lewis structure. Therefore, there exists more than one Lewis structure for representing a molecule or ion. These structures are known as resonance structures. These are the hypothetical structures and do not specify the exact structure. These resonance structure combine together to give resonance hybrid that is lower in energy and is the most stable structure.
The delocalization of electrons results in the formation resonance structure.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
Draw the three possible resonance structures for an acid bromide, RCOBr. Then decide if RCOBr is more or less stabilized by resonance than a carboxylic acid (RCOOH).
give an example of a nucleophilic substitution reaction with chlorohexane
Explain why aldehydes and ketones react with a weak acid such as hydrogen cyanide but do not react with strong acids such as HCl or H2SO4 (other than being protonated by them).
Chapter 13 Solutions
ORG CHEM CONNECT CARD
Ch. 13.1 - Prob. 1PCh. 13.1 - Prob. 2PCh. 13.2 - Prob. 3PCh. 13.3 - Prob. 4PCh. 13.3 - Prob. 5PCh. 13.4 - Prob. 7PCh. 13.5 - Problem 15.8 Which bond in the each compound is...Ch. 13.6 - Prob. 9PCh. 13.6 - Prob. 10PCh. 13.7 - Prob. 11P
Ch. 13.7 - Prob. 12PCh. 13.8 - Prob. 13PCh. 13.8 - Prob. 14PCh. 13 - Prob. 27PCh. 13 - Prob. 28PCh. 13 - Prob. 34PCh. 13 - 15.37 What alkane is needed to make each alkyl...Ch. 13 - 15.38 Which alkyl halides can be prepared in good...Ch. 13 - Prob. 37PCh. 13 - 15.40 Explain why radical bromination of p-xylene...Ch. 13 - a. What product(s) (excluding stereoisomers) are...Ch. 13 - Prob. 40PCh. 13 - 15.43 Draw the products formed when each alkene is...Ch. 13 - 15.44 Draw all constitutional isomers formed when...Ch. 13 - 15.45 Draw the organic products formed in each...Ch. 13 - Prob. 45PCh. 13 - 15.47 Treatment of a hydrocarbon A (molecular...Ch. 13 - 15.48 Draw the products formed in each reaction...Ch. 13 - 15.53 Consider the following bromination: .
a....Ch. 13 - 15.54 Draw a stepwise mechanism for the following...Ch. 13 - Prob. 57PCh. 13 - 15.57 Devise a synthesis of each compound from...Ch. 13 - Prob. 59PCh. 13 - Prob. 60PCh. 13 - 15.60 Devise a synthesis of each compound using ...Ch. 13 - Prob. 62PCh. 13 - Prob. 63PCh. 13 - 15.63 As described in Section 9.16, the...Ch. 13 - 15.64 Ethers are oxidized with to form...
Knowledge Booster
Learn more about
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
- Radicals and carbocations are electrophiles. Define how and why ?arrow_forwardComplete the reaction of propylene oxide with methylaminearrow_forward16. Draw significant resonance structures for the following compound. Which of this is/are most significant resonance structure(s)? Explain why. (a) مهم (b) the H H- (c)arrow_forward
- Explain two different ways to introduce an alkyl group on a benzene ring ?arrow_forward2.) Cyclohexane Why insoluble in water? Why insoluble in HCl? Why insoluble in NaOH? Why insoluble in NaHCO?arrow_forward4. Given the following condensed structural formulas, a) draw the skeletal structures of each molecule and place partial charges on atoms in the reactive functional group, b) label each as an expected nucleophile or electrophile based on charges, e) determine if the molecule could be described as a Lewis acid (electron pair acceptor) or a Lewis base (electron pair donor). i) NaC=CCH3 ii) C6HsCHO iii) CH3CH₂COOHarrow_forward
- Homolysis of the indicated C–H bond in propene forms a resonancestabilizedradical. Question: Draw the two possible resonance structures for this radical.arrow_forwardPhenol and other derivatives with a single hydroxyl group on the aromatic ring are not easily oxidized to form a ketone. Why is this? Select all that apply: O Phenol is a secondary alcohol; secondary alcohols do not oxidize. O The carbon that the hydroxyl group is attached to in phenol does not have a hydrogen attached. Forming a double bond between the oxygen and the carbon would require breaking up the stable aromatic ring. Phenol is a tertiary alcohol, which does not oxidize.arrow_forwardExplain why methyl trifluoroacetate, CF3CO2CH3, is more reactive than methyl acetate, CH3CO2CH3, in nucleophilic acyl substitution reactions.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning