Skip to main content
Ch.21 - Organic Chemistry
Tro - Chemistry: A Molecular Approach 4th Edition
Tro4th EditionChemistry: A Molecular ApproachISBN: 9780134112831Non è quello che usi tu?Cambia libro di testo
Capitolo 21, Problema 34

Based on the molecular formula, determine whether each com- pound is an alkane, alkene, or alkyne. (Assume that the hydro- carbons are noncyclical and there is no more than one multiple bond.)
a. C8H16 b. C4H6 c. C7H16 d. C2H2

Guida verificata passo dopo passo
1
Determine the general formula for alkanes, which is C_nH_{2n+2}.
Determine the general formula for alkenes, which is C_nH_{2n}.
Determine the general formula for alkynes, which is C_nH_{2n-2}.
For each compound, compare its molecular formula to the general formulas for alkanes, alkenes, and alkynes.
Classify each compound based on which general formula it matches.

Risposta video verificata per un problema simile:

Questa soluzione video è stata consigliata dai nostri tutor come utile per risolvere questo problema.
Durata del video:
4m

Concetti chiave

Ecco i concetti essenziali che devi comprendere per rispondere correttamente alla domanda.

Hydrocarbon Classification

Hydrocarbons are organic compounds consisting solely of hydrogen and carbon. They are classified into three main categories: alkanes (single bonds), alkenes (at least one double bond), and alkynes (at least one triple bond). Understanding the type of bonds present in a hydrocarbon is essential for determining its classification.
Video consigliato:
Percorso guidato
04:29
Intro To Hydrocarbons

General Formula for Hydrocarbons

Each class of hydrocarbons has a general formula that helps identify their structure. Alkanes follow the formula CnH2n+2, alkenes follow CnH2n, and alkynes follow CnH2n-2. By comparing the molecular formula of a compound to these general formulas, one can ascertain whether it is an alkane, alkene, or alkyne.
Video consigliato:
Percorso guidato
04:29
Intro To Hydrocarbons

Degree of Unsaturation

The degree of unsaturation indicates the number of rings and multiple bonds in a hydrocarbon. 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 higher degree of unsaturation suggests the presence of double or triple bonds, which is crucial for classifying the compound.
Video consigliato:
Percorso guidato
02:12
Saturated and Unsaturated Hydrocarbons