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Ch.21 - Organic Chemistry
Tro - Chemistry: A Molecular Approach 4th Edition
Tro4th EditionChemistry: A Molecular ApproachISBN: 9780134112831당신이 사용하는 게 아니라요?교과서 변경
21장, 문제 33

Based on the molecular formula, determine whether each compound is an alkane, alkene, or alkyne. (Assume that the hydrocarbons are noncyclical and there is no more than one multiple bond.) a. C5H12 b. C3H6 c. C7H12 d. C11H22

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1
insert step 1> Determine the general formula for each type of hydrocarbon: alkanes (C_nH_{2n+2}), alkenes (C_nH_{2n}), and alkynes (C_nH_{2n-2}).
insert step 2> For compound a (C5H12), compare the molecular formula to the general formulas. Check if it fits C_nH_{2n+2} for alkanes.
insert step 3> For compound b (C3H6), compare the molecular formula to the general formulas. Check if it fits C_nH_{2n} for alkenes.
insert step 4> For compound c (C7H12), compare the molecular formula to the general formulas. Check if it fits C_nH_{2n} for alkenes.
insert step 5> For compound d (C11H22), compare the molecular formula to the general formulas. Check if it fits C_nH_{2n} for alkenes.

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주요 개념

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Hydrocarbons

Hydrocarbons are organic compounds consisting entirely of hydrogen and carbon atoms. They can be classified into three main categories: alkanes, alkenes, and alkynes, based on the types of bonds between carbon atoms. Alkanes contain only single bonds, alkenes have at least one double bond, and alkynes contain at least one triple bond.
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Intro To Hydrocarbons

General Formula for Hydrocarbons

Each class of hydrocarbons has a general formula that helps identify their structure. Alkanes follow the formula CnH(2n+2), alkenes follow CnH(2n), and alkynes follow CnH(2n-2). By comparing the molecular formula of a compound to these general formulas, one can determine its classification as an alkane, alkene, or alkyne.
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가이드 코스
04:29
Intro To Hydrocarbons

Degree of Unsaturation

The degree of unsaturation indicates the number of rings and multiple bonds in a hydrocarbon molecule. It can be calculated using the formula: Degree of Unsaturation = (2C + 2 + N - H - X)/2, where C is the number of carbons, N is the number of nitrogens, H is the number of hydrogens, and X is the number of halogens. A degree of unsaturation greater than zero suggests the presence of double or triple bonds.
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Saturated and Unsaturated Hydrocarbons