Question: Draw the products of each combustion reaction.

a.

b.

Short Answer

Expert verified

Answer

a. CH3CH2CH3+5O2Flame3CO2+4H2O+Heat

b.

Step by step solution

01

Combustion reaction

Combustion is a type of oxidation reaction.

Hydrocarbons burn in the presence of oxygen to produce carbon dioxide and water. The combustion reaction also releases a lot of heat energy.

Due to the release of a lot of heat energy during combustion,

many alkanes are used as fuels in natural gas, gasoline, etc.

The combustion reaction of all hydrocarbons always results in the formation of same products, which are carbon dioxide and water.

02

Products of the combustion reaction

a. The following reaction is the combustion of propane. It reacts with oxygen to produce carbon dioxide and water, as shown below:

CH3CH2CH3+5O2Flame3CO2+4H2O+Heat

b. The following reaction is the combustion of cyclohexane. It also reacts with oxygen to form carbon dioxide and water, as shown below:

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Question: a.Draw the three staggered and three eclipsed conformations that result from rotation around the bond labeled in red using Newman projections. b. Label the most stable and least stable conformation.

Question: For cis-1,3-diethylcyclobutane, draw (a) a stereoisomer; (b) a constitutional isomer.

Question: Draw the structure corresponding to each IUPAC name.

a. 3-ethyl-2-methylhexane

b. sec-butylcyclopentane

c. 4-isopropyl-2,4,5-trimethylundecane

d. cyclobutylcycloheptane

e. 3-ethyl-1,1-dimethylcyclohexane

f. 4-butyl-1,1-diethylcyclooctane

g. 6-isopropyl-2,3-dimethyldodecane

h. 2,2,6,6,7-pentamethyloctane

i. cis-1-ethyl-3-methylcyclopentane

j. trans-1-tert-butyl-4-ethylcyclohexane

Question: Answer the following questions about compound A, which contains a -CH3group and OH group bonded to the carbon skeleton that consists of three six-membered rings in the conformation shown.

a. Are the -CH3and OH groups oriented cis or trans to each other?

b. Is a substituent on localid="1648626189057" Cathat is cis to the CH3 group located in the axial or equatorial position?

c. Is an equatorial Br at Cboriented cis or trans to the OH group?

d. Is the H atom on Cclocated cis or trans to the OH group?

e. Is a substituent on Cdthat is trans to the OH group located in the axial or equatorial position?

Question: Consider the tricyclic structure B.

(a) Label each substituent on the rings as axial or equatorial.

(b) Draw B using chair conformations for each six-membered ring.

(c) Label the atoms on the ring fusions (the carbons that join each set of two rings together) as cis or trans to each other.

B

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free