Bundle: Introduction to General, Organic and Biochemistry, 11th + OWLv2, 4 terms (24 months) Printed Access Card
11th Edition
ISBN: 9781305705159
Author: Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher: Cengage Learning
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Question
Chapter 10, Problem 10.38P
a)
Interpretation Introduction
Interpretation:
To draw the structural formula for four primary
Concept Introduction:
The atoms in a molecule form bonds which are represented by the lines that show the structural formula omitting the carbon and hydrogen bonds is known as the structural formula.b)
Interpretation Introduction
Interpretation:
To draw the structural formula for three secondary amines with the molecular formula
Concept Introduction:
The atoms in a molecule form bonds which are represented by the lines that show the structural formula omitting the carbon and hydrogen bonds is known as the structural formula.
c)
Interpretation Introduction
Interpretation:
To draw the structural formula for one tertiary amine with the molecular formula
Concept Introduction:
The atoms in a molecule form bonds which are represented by the lines that show the structural formula omitting the carbon and hydrogen bonds is known as the structural formula.
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Students have asked these similar questions
Classify the amine below by its degree.
H3C-NH2-CH3
Select the correct answer below:
primary amine
secondary amine
tertiary amine
quaternary amine
Draw structural formulas for
Q.) The four primary (1°) amines with the molecular formula C4H11N.
1. Which statement best described the ability of amines to hydrogen bond?
A. Primary, secondary and tertiary amines can all hydrogen bond with molecules identical to themselves.
B. Primary and secondary amines can hydrogen bond with molecules identical to themselves, but tertiary amines cannot.
C. Only primary amines can hydrogen bond with molecules identical to themselves. Secondary and tertiary amines cannot.
D. Primary, secondary and tertiary amines cannot hydrogen bond with molecules identical to themselves, but the can hydrogen bond with water.
Chapter 10 Solutions
Bundle: Introduction to General, Organic and Biochemistry, 11th + OWLv2, 4 terms (24 months) Printed Access Card
Ch. 10.3 - Prob. 10.1PCh. 10.4 - Prob. 10.2PCh. 10.4 - Prob. 10.3PCh. 10.4 - Prob. 10.4PCh. 10.4 - Prob. 10.5PCh. 10.4 - Prob. 10.6PCh. 10 - Prob. 10.7PCh. 10 - Prob. 10.8PCh. 10 - 10-9 Is there any difference between vanillin made...Ch. 10 - Prob. 10.10P
Ch. 10 - 10-11 What important experiment did Wohler carry...Ch. 10 - Prob. 10.12PCh. 10 - Prob. 10.13PCh. 10 - Prob. 10.14PCh. 10 - 10-15 How many electrons are in the valence shell...Ch. 10 - 10-16 What is the relationship between the number...Ch. 10 - Prob. 10.17PCh. 10 - Prob. 10.18PCh. 10 - 10-19 Write Lewis structures for these ions. (a)...Ch. 10 - 10-20 Why are the following molecular formulas...Ch. 10 - 10-21 Explain how to use the valence-shell...Ch. 10 - 10-22 Suppose you forget to take into account the...Ch. 10 - Suppose you forget to take into account the...Ch. 10 - 10-24 Use the VSEPR model to predict the bond...Ch. 10 - Prob. 10.25PCh. 10 - Prob. 10.26PCh. 10 - 10-27 What is meant by the term functional group?Ch. 10 - 10-28 List three reasons why functional groups are...Ch. 10 - Prob. 10.29PCh. 10 - Prob. 10.30PCh. 10 - Prob. 10.31PCh. 10 - 10-32 Draw a structural formula for the one...Ch. 10 - 10-33 What is the meaning of the term tertiary (...Ch. 10 - Prob. 10.34PCh. 10 - Draw structural formulas for each of the...Ch. 10 - 10-36 Draw structural formulas for the six ketones...Ch. 10 - 10-37 Draw structural formulas for the eight...Ch. 10 - Prob. 10.38PCh. 10 - 10-39 (Chemical Connections 10A) How was Taxol...Ch. 10 - Prob. 10.40PCh. 10 - Prob. 10.41PCh. 10 - Silicon is immediately below carbon in Group 4A of...Ch. 10 - 10-43 Phosphorus is immediately below nitrogen in...Ch. 10 - Draw the structure for a compound with the...Ch. 10 - 10-45 Draw structural formulas for the eight...Ch. 10 - Prob. 10.46PCh. 10 - 10-47 Which of these covalent bonds are polar, and...Ch. 10 - Of the bonds in Problem 10-47, which is the most...Ch. 10 - Prob. 10.49PCh. 10 - Prob. 10.50PCh. 10 - Following is a structural formula for naphthalene....Ch. 10 - Prob. 10.52PCh. 10 - Prob. 10.53PCh. 10 - Urea, (NH.,)2CO, is used in plastics and in fertil...Ch. 10 - Prob. 10.55PCh. 10 - Prob. 10.56PCh. 10 - Aspirin is prepared by the reaction of salicylic-...Ch. 10 - Following is the structural formula of acetamide....Ch. 10 - Prob. 10.59P
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Similar questions
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- Propose structures for amines that fit these descriptions:(a) A secondary amine with formula C5H13N(b) A tertiary amine with formula C6H13N(c) A cyclic quaternary amine that has the formula C6H14N+arrow_forwardBecause amines are basic, they can often accept a proton. Draw the protonated structure of n-propylamine.arrow_forwardDraw and name compounds that meet the following descriptions: a. Two primary, 2 secondary, and 2 tertiary amines having the formula C5H13Narrow_forward
- Q.The angle found in p-nitroaniline means that the amine group is planar and in the same plane as the benzene ring. Why is this the case? 1. The nitro group withdraws the lone pair electrons from the amine, primarily via induction, making the N atom sp2 hybridized and hence trigonal planar. 2. The nitro group withdraws the lone pair electrons from the amine, primarily via resonance, making the N atom sp2 hybridized and hence trigonal planar. 3. The lone pair of the N atom of the NH2 must be in a p orbital to make the system aromatic. 4. The nitrogen of an amine is usually planar, and aniline and methylamine are exceptions.arrow_forwardDraw structures of four different amides with molecular formula C3H7NO.arrow_forward2. What is produced when an amine reacts with a strong acid such as HCl? A. An amine and the OH- ion B. An amide and the H+ ion C. An ammonium hydroxide D. An ammonium saltarrow_forward
- 回答所有问题，包括5a），5b），6a），6b） 5a），5b）是相互关联的 6a），6b）是相互关联的 5a) How do the boiling points of aldehydes, ketones, alcohols and hydrocarbonscompare when they have the same or similar numbers of carbons? 5b) Explain the reasons for these differences. 6a) For the three different amines in this experiment, how does the number of hydrogen atoms bound to the nitrogen affect the boiling point?6b) Explain this trend.arrow_forwardCharacterize each compound in terms of functional groups (primary amine, secondary amine, tertiary amine). 1. Propylamine 2. Ethylmethylamine 3. Trimethylamine 4. Butylamine 5. Anilinearrow_forward1. Use the image provided to answer the question in detail: a) Two of the earliest drug molecules featured in Chapter 8 are Vicodin and Heroin, whose chemical structures are very similar. Both of these molecules contain an amine functional group and several rings. Indicate the number of aromatic rings in each structure, and identify the amine functional group in each molecule as primary, secondary, or tertiary.arrow_forward
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