GENERAL,ORGANIC, & BIOLOGICAL CHEM-ACCES
4th Edition
ISBN: 9781265982959
Author: SMITH
Publisher: MCG
expand_more
expand_more
format_list_bulleted
Question
Chapter 14, Problem 75P
Interpretation Introduction
(a)
Interpretation:
The disulfide formed on oxidizing the following thiol should be determined:
Concept Introduction:
Thiols are organic compounds which contains a sulfhydryl group (SH group) bonded to a tetrahedral carbon.
Reaction of thiols with oxidizing agent will form disulfides and the reaction is known as an oxidation reaction.
Interpretation Introduction
(b)
Interpretation:
The disulfide formed on oxidizing the following thiol should be determined:
Concept Introduction:
Thiols are organic compounds which contains a sulfhydryl group (SH group) bonded to a tetrahedral carbon.
Reaction of thiols with oxidizing agent will form disulfides and the reaction is known as an oxidation reaction.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
If a radiation intensity l0 = 2.5x1010 fotones s-1 cm2 causes a dissolución and an absorbance of 0.95 will be recorded. How much incident radiation is absorbed by the music screen?
From the causes of the detection of a spectral band of a spectrum obtained by a signal in the gaseous phase that is indicated, you can avoid or minimize those that have their origin in:a) the Doppler effectb) collisionsc) the life time of the excited state
a) Why is it possible that all types of atoms occupy the fundamental energy level?b) What should be the value of the participation function so that it occurs?c) keep in mind that the translational levels of a system are very close, which must be the condition that tenga lugar el condensado de átomos en el fundamental level?
Chapter 14 Solutions
GENERAL,ORGANIC, & BIOLOGICAL CHEM-ACCES
Ch. 14.1 - Prob. 14.1PCh. 14.2 - Prob. 14.1PPCh. 14.2 - Classify each hydroxyl group in sorbitol as 1°,...Ch. 14.2 - Prob. 14.3PCh. 14.2 - Prob. 14.4PCh. 14.3 - Prob. 14.2PPCh. 14.3 - Give the structure corresponding to each name a....Ch. 14.5 - Draw the products formed when each alcohol is...Ch. 14.5 - Prob. 14.6PCh. 14.5 - Prob. 14.7P
Ch. 14.5 - Prob. 14.4PPCh. 14.6 - Prob. 14.8PCh. 14.7 - Prob. 14.9PCh. 14.7 - Prob. 14.5PPCh. 14.7 - Prob. 14.10PCh. 14.7 - Name each ether. CH3OCH2CH2CH2CH3Ch. 14.7 - Prob. 14.11PCh. 14.8 - (a) Translate the hall and stick model of...Ch. 14.8 - Prob. 14.13PCh. 14.9 - Prob. 14.14PCh. 14.9 - Prob. 14.15PCh. 14.9 - Prob. 14.16PCh. 14.9 - Prob. 14.17PCh. 14.9 - Prob. 14.18PCh. 14.9 - Prob. 14.19PCh. 14.9 - Prob. 14.20PCh. 14.10 - Give the IUPAC name for each thiol.Ch. 14.10 - Prob. 14.21PCh. 14.10 - Prob. 14.22PCh. 14 - Classify each alcohol as 1°, 2°, or 3o a....Ch. 14 - Prob. 24PCh. 14 - Prob. 25PCh. 14 - Classify each halide hi A as 1°, 2°, or 3°. A is a...Ch. 14 - Prob. 27PCh. 14 - Draw the structure of a molecule that fits each...Ch. 14 - Draw the structure of the six constitutional...Ch. 14 - Draw the structure of the four constitutional...Ch. 14 - Draw the structure of l-propanethiol, a compound...Ch. 14 - Prob. 32PCh. 14 - Prob. 33PCh. 14 - Prob. 34PCh. 14 - Prob. 35PCh. 14 - Answer each question about alcohol B. Draw a...Ch. 14 - Prob. 37PCh. 14 - Give the IUAPC name for each alcohol.Ch. 14 - Prob. 39PCh. 14 - Prob. 40PCh. 14 - Prob. 41PCh. 14 - Prob. 42PCh. 14 - Draw the structures and give the IUPAC names for...Ch. 14 - Prob. 44PCh. 14 - Prob. 45PCh. 14 - Prob. 46PCh. 14 - Give the structure corresponding to each IUPAC...Ch. 14 - Give the structure corresponding to each IUPAC...Ch. 14 - Which compound in each pair has the higher boiling...Ch. 14 - Rank the compounds in order of increasing melting...Ch. 14 - Rank the following compounds in order of...Ch. 14 - Rank the following compounds in order of...Ch. 14 - Prob. 53PCh. 14 - Prob. 54PCh. 14 - Prob. 55PCh. 14 - Prob. 56PCh. 14 - Prob. 57PCh. 14 - Prob. 58PCh. 14 - Prob. 59PCh. 14 - Prob. 60PCh. 14 - Prob. 61PCh. 14 - Prob. 62PCh. 14 - Prob. 63PCh. 14 - Prob. 64PCh. 14 - Prob. 65PCh. 14 - Prob. 66PCh. 14 - Prob. 67PCh. 14 - Prob. 68PCh. 14 - Prob. 69PCh. 14 - Prob. 70PCh. 14 - Prob. 71PCh. 14 - Prob. 72PCh. 14 - Prob. 73PCh. 14 - Prob. 74PCh. 14 - Prob. 75PCh. 14 - Prob. 76PCh. 14 - Prob. 77PCh. 14 - Prob. 78PCh. 14 - Prob. 79PCh. 14 - Prob. 80PCh. 14 - With reference to the halogenated organic...Ch. 14 - Prob. 82PCh. 14 - Prob. 83PCh. 14 - Prob. 84PCh. 14 - Write out the chemical reaction that occurs when a...Ch. 14 - Prob. 86PCh. 14 - Prob. 87PCh. 14 - Lactic acid [CH3CH(OH)CO2H] gives sour milk its...Ch. 14 - Prob. 89PCh. 14 - Prob. 90PCh. 14 - Prob. 91PCh. 14 - Prob. 92PCh. 14 - Prob. 93PCh. 14 - Answer the following questions about alcohol B....Ch. 14 - Prob. 95CPCh. 14 - Dehydration of alcohol C forms two products of...
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
- At the polar moment of Rnm transition, you can confirm thata) nunca can be ser 0b) is a very important magnitude in Raman spectroscopyc) is related to the probability of spectroscopic transactionsd) is related to the selection rulesarrow_forwardIn Fourier transformed spectroscopya) use a very sensitive monocromador systemb) the detection time is inferior to conventional spectroscopiac) the signal is detected depending on the frequencyd) occurs simultaneously at all frequency intervalsarrow_forwardIf a radiation intensity l0 = 2.5x1010 fotones s-1cm2 results in a dissolución, an absorption of 0.95 will be recorded. What is the percentage of incident radiation and transmission?a) 88.88% b) 5% c) 11.22% d) 95%arrow_forward
- Indicate the spectroscopic transmission that requires greater energy radiation. Justification:a) NMR b) vibration c) electronica d) rotationarrow_forwardAfter an induced absorption process of an intensity, there are (without population inversion) transitions between:a) vibrational and rotational levels in the infrared region, we obtainb) vibrational levels exclusively in the infrared regionc) vibrational and rotational levels in the microwave regiond) transitions between nuclear spin levels in the radio frequency regionarrow_forwardIn a spontaneous emission process:a) the ground state population decreasesb) the excited state population decreasesc) the non-radiative component is predominantd) the emitted radiation is coherentarrow_forward
- For a molecule there are 3 energy levels A, B and C, where B is an intermediate energy level between A and C. The A → C transition occurs at 480 nm and the B → C transition occurs at 885 nm. Indicate the wavelength at which the A → B transition will occur.arrow_forwardFor a molecule there are three energy levels: A, B and C. If the transition A → B occurs at 1049 nm and the transition B → C occurs at 885 nm, we can say that the wavelength of the transition A → C will occur at approximately:a) 164 nm b) 1934 nm c) 480 nm d) 967 nmarrow_forward: Naming the Alkanes a) Write the IUPAC nomenclature of the compound below b) Draw 4-isopropyl-2,4,5-trimethylheptane, identify the primary, secondary, tertiary, and quaternary carbons. c) Rank pentane, neopentane and isopentane for boiling point. pentane: H3C-CH2-CH2-CH2-CH3 neopentane: CH3 H3C-C-CH3 isopentane: CH3 CH3 H3C-CH2-CH-CH3arrow_forward
- An essential part of the experimental design process is to select appropriate dependent and independent variables. True Falsearrow_forward10.00 g of Compound X with molecular formula C₂Hg are burned in a constant-pressure calorimeter containing 40.00 kg of water at 25 °C. The temperature of the water is observed to rise by 2.604 °C. (You may assume all the heat released by the reaction is absorbed by the water, and none by the calorimeter itself.) Calculate the standard heat of formation of Compound X at 25 °C. Be sure your answer has a unit symbol, if necessary, and round it to the correct number of significant digits.arrow_forwardneed help not sure what am doing wrong step by step please answer is 971A During the lecture, we calculated the Debye length at physiological salt concentrations and temperature, i.e. at an ionic strength of 150 mM (i.e. 0.150 mol/l) and a temperature of T=310 K. We predicted that electrostatic interactions are effectively screened beyond distances of 8.1 Å in solutions with a physiological salt concentration. What is the Debye length in a sample of distilled water with an ionic strength of 10.0 µM (i.e. 1.00 * 10-5 mol/l)? Assume room temperature, i.e. T= 298 K, and provide your answer as a numerical expression with 3 significant figures in Å (1 Å = 10-10 m).arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Introductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
- Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage LearningChemistry by OpenStax (2015-05-04)ChemistryISBN:9781938168390Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark BlaserPublisher:OpenStax
Introductory Chemistry: A Foundation
Chemistry
ISBN:9781337399425
Author:Steven S. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
Chemistry by OpenStax (2015-05-04)
Chemistry
ISBN:9781938168390
Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:OpenStax
07 Physical Properties of Organic Compounds; Author: Mindset;https://www.youtube.com/watch?v=UjlSgwq4w6U;License: Standard YouTube License, CC-BY