EBK GENERAL, ORGANIC, & BIOLOGICAL CHEM
3rd Edition
ISBN: 9781259298424
Author: SMITH
Publisher: VST
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Chapter 18, Problem 18.76P
Interpretation Introduction
Interpretation:
Concept introduction:
2-phenylethylamine is a primary amine with 2 carbons where a phenyl group has been substituted in the 2nd carbon.
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Students have asked these similar questions
Which of the following amines are derivatives of 2-phenylethylamine? Label the atoms of 2-phenylethylamine in those amines that contain this unit.
Write the names for the amines using the naming styles taught in the McMurry text.
H2
H3C-N-C-CH3
name:
H2
H2
H3C-C-Ņ-c-CH3
H
name:
These compounds are
amines.
is this molecule a primary amine? explain in your own words
Chapter 18 Solutions
EBK GENERAL, ORGANIC, & BIOLOGICAL CHEM
Ch. 18.1 - Prob. 18.1PCh. 18.1 - Prob. 18.2PCh. 18.1 - Prob. 18.3PCh. 18.1 - Prob. 18.4PCh. 18.2 - Prob. 18.5PCh. 18.2 - Prob. 18.6PCh. 18.2 - Prob. 18.7PCh. 18.3 - Prob. 18.8PCh. 18.4 - Decaffeinated coffee is produced by extracting the...Ch. 18.4 - Prob. 18.10P
Ch. 18.5 - Prob. 18.11PCh. 18.5 - Prob. 18.12PCh. 18.5 - Prob. 18.13PCh. 18.6 - Prob. 18.14PCh. 18.6 - Prob. 18.15PCh. 18.6 - Prob. 18.16PCh. 18.6 - Name each ammonium salt. a. ( CH3 NH3)+Cl b. [( CH...Ch. 18.6 - Prob. 18.18PCh. 18.6 - Prob. 18.19PCh. 18.7 - Prob. 18.20PCh. 18.7 - Prob. 18.21PCh. 18.8 - Prob. 18.22PCh. 18.8 - Prob. 18.23PCh. 18.8 - Prob. 18.24PCh. 18.9 - Prob. 18.25PCh. 18.9 - Prob. 18.26PCh. 18.9 - Prob. 18.27PCh. 18.10 - Prob. 18.28PCh. 18 - Prob. 18.29PCh. 18 - Prob. 18.30PCh. 18 - Prob. 18.31PCh. 18 - Prob. 18.32PCh. 18 - Prob. 18.33PCh. 18 - Prob. 18.34PCh. 18 - Prob. 18.35PCh. 18 - Prob. 18.36PCh. 18 - Prob. 18.37PCh. 18 - Prob. 18.38PCh. 18 - Give an acceptable name for each amine. a. b.Ch. 18 - Give an acceptable name for each amine. a. b.Ch. 18 - Give an acceptable name for each amine. a. b. c....Ch. 18 - Give an acceptable name for each amine. a. CH3(...Ch. 18 - Prob. 18.43PCh. 18 - Prob. 18.44PCh. 18 - Prob. 18.45PCh. 18 - Prob. 18.46PCh. 18 - Prob. 18.47PCh. 18 - Prob. 18.48PCh. 18 - Prob. 18.49PCh. 18 - Prob. 18.50PCh. 18 - Which compound in each pair has the higher boiling...Ch. 18 - Which compound in each pair has the higher boiling...Ch. 18 - Draw the hydrogen-bonding interactions that occur...Ch. 18 - Prob. 18.54PCh. 18 - Prob. 18.55PCh. 18 - Which compound has the higher water solubility:...Ch. 18 - Prob. 18.57PCh. 18 - Prob. 18.58PCh. 18 - Draw the products of each acid-base reaction. a....Ch. 18 - Draw the products of each acid-base reaction. a....Ch. 18 - Prob. 18.61PCh. 18 - Prob. 18.62PCh. 18 - What type of nitrogen heterocycle occurs in both...Ch. 18 - Only one of the N atoms in nicotine has a trigonal...Ch. 18 - Prob. 18.65PCh. 18 - Prob. 18.66PCh. 18 - Why are aqueous solutions of an alkaloid slightly...Ch. 18 - Prob. 18.68PCh. 18 - Prob. 18.69PCh. 18 - Explain why patients with Parkinson’s disease...Ch. 18 - Prob. 18.71PCh. 18 - Prob. 18.72PCh. 18 - Prob. 18.73PCh. 18 - Prob. 18.74PCh. 18 - Prob. 18.75PCh. 18 - Prob. 18.76PCh. 18 - Prob. 18.77PCh. 18 - Prob. 18.78PCh. 18 - Prob. 18.79PCh. 18 - Prob. 18.80PCh. 18 - Prob. 18.81PCh. 18 - Prob. 18.82PCh. 18 - Prob. 18.83PCh. 18 - Prob. 18.84PCh. 18 - Prob. 18.85PCh. 18 - Prob. 18.86PCh. 18 - Prob. 18.87PCh. 18 - Why do some antihistamines cause drowsiness while...Ch. 18 - Prob. 18.89PCh. 18 - Prob. 18.90PCh. 18 - Compare the structures of morphine and heroin....Ch. 18 - Prob. 18.92CP
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Similar questions
- Write the systematic (IUPAC) names for the amines. The names should have the format alkanamine. H,C-N-CH-CH, systematic (IUPAC) name: NH–CH, H,C-CH-CH-CH, systematic (IUPAC) name: These compounds are secondary amines.arrow_forwardWrite structural formulas for these amines. a)Cyclohexylmethylaminearrow_forwardBriefly explain primary, secondary, tertiary, and quarternary amine structures.arrow_forward
- Write the systematic (IUPAC) names for the amines. The names should have the format alkanamine. H₂C-N-CH3 H3C-CH2-CH-CH3 systematic (IUPAC) name: HC-N-CH2-CH3 HC-CH2-CH2-CH₂ systematic (IUPAC) name: These compounds are amines.arrow_forwardComplete this table for different amine compounds. Chemical propylamine quaternary ammonium ion methylphenylamine Molecular formula C3H9N C₂H7N C5H13N C4H10N Structural formula (CH3)3N (CH3)2NH CH 3 I (CH₂) 11 | H3C(CH2) 11 -N-(CH₂)11CH3 NHCH3 (CH₂)11 CH3 CH3CH2CH2-NH-CH3 + Classification Tertiary Quaternary Tertiary Secondaryarrow_forwardFollowing amines can be classified as -- and ---, respectively. HN-CH3 H3C-CH3 'N' H primary amine, secondary amine secondary amine, ammonium salt secondary amine, primary amine secondary amine, tertiary aminearrow_forward
- Draw structural formulas for all the amines having the formula C3H9N. Classify each as either a primary amine, a secondary amine, or a tertiary amine.arrow_forwardWhich compound is a primary amine with the formula C5H13N? * H2N H2N II III NH2 IV V IV O II O III and V d、飞arrow_forward1. 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.arrow_forward
- The following molecular formulas represent saturated amine compounds or unsaturated amine compounds that contain C=C bonds. Determine whether each compound is saturated and how many C=C bonds are present. a C,H1N This amine is c and contains C=C bond(s). b C,H12N2 correct lamine is and contains C-C bond(s). € CH,N This amine is and contains C=C bond(s).arrow_forwardSketch the product, Then writeh the IUPAC NAME OF THE AMINE PRODUCT and the dominant Intermolecular force for the product. CH, NH, + H -CI O CH3-NH3*Cr, methylammonium chloride (Amine Product: H-Bond) O CH3-CH3-NH3*Cl', ethylammonium chloride (Amine Product: H-Bond) O CH3-NH3*, methylammonium ion (Amine Product: Dipole-Dipole) +. O CH3-NH3*CI , ethylammonium chloride (Amine Product: H-Bond) O CH3-NH3*CI', ethylammonium chloride (Amine Product: Dipole-Dipole) CH3-NH3*Cl", methylammonium chloride (Amine Product: lonic)arrow_forwardWhat is the generic structure of amines? Write the structures of two specific amines.arrow_forward
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