However, safety concerns by many teachers and availability of equipment in some schools mean that this key and. Catalysis is again needed to describe the dehydration of alcohols to form alkenes in wm, and the friedelcrafts alkylation and acylation of arenes in cd. This is being formed either by removal of a hydride ion or by addition of a proton. The reaction between alkanes and chlorine or bromine. As the alkanes get shorter their boiling point decreases so each fraction condenses at a different temperature. Steam cracking is a petrochemical process in which saturated hydrocarbons are broken down into smaller, often unsaturated, hydrocarbons. Gcse chemistry what is the cracking of hydrocarbons. Many of the substances with longer molecules produced from the fractional distillation of crude oil are cracked. The apparent rate coefficient for alkane cracking was described as the product of the number of alkane molecules per unit mass of zeolite that are close enough to a bronstedacid site to be in the reactant state for the cleavage of a specific c. The alkane is brought into contact with the catalyst at a temperature of about 500c and moderately low pressures. They need different conditions and are used to produce different products produces mostly alkenes e. Cracking hydrocarbons in liquid paraffin with a catalyst resource. Also attached are differentiated sheets to assist students with understanding the different methods of cracking thermal steam and catalytic.
Graded with a video link and mark schemes for everything. Cracking hydrocarbons on a microscale resource rsc education. Thus, cracking long alkane molecules helps to supply the world with shorter alkane molecules. Modern lowtemperature hydrocracking was put into commercial production in 1963.
Practical will take the entire lesson to explain, set up and complete plenary. A cracking practical can be carried out in a school lab quite easily by using a broken pottery as a catalyst. Cracking is used to convert long alkanes into shorter, more useful hydrocarbons. Cracking the hydrocarbons in paraffin to form shorter alkanes and alkenes can be done as a class practical. Branched alkanes containing three or more carbon atoms in their longest chain have isomers with unique names iii. An introduction to the alkanes including cycloalkanes and their physical properties. Cracking and alkenes crude oil, hydrocarbons and alkanes aqa. A brief look at cracking alkanes in the oil industry. Experiments about physical and chemical properties of alkanes investigating the solubility of hexane in water and the action of some common reagents on hexane i. Preparation of alkanes from unsaturated hydrocarbons. The ethene and propene are important materials for making plastics or producing other organic chemicals.
Alkanes formula, definition, structure, properties, videos. Cracking is the name given to breaking up large hydrocarbon molecules into smaller and more useful bits. The worksheet can also be found by clicking on the worksheet below. Cracking of alkanes cracking is a form of thermal decomposition, which breaks long chain hydrocarbons, many of which are not very useful, into shorter molecules by heating them. Hydrocarbon properties a physical properties b chemical properties related to chemical reactions. Branched alkanes contain only carbon and hydrogen c and h. A systematic method for the naming of many organic compounds is contained in the iupac publication. There are two aspects of this industrial, and in the lab.
Alkanes which has around 35 long chains or more the carbon atom are usually found in asphalt that are used for the surface of a road. Alkanes alkanes are saturated hydrocarbons contain single. Cracking and alkenes crude oil, hydrocarbons and alkanes. The following are some examples for linear alkanes. Cracking reactions use heat andor a catalyst to crack alkanes, breaking carboncarbon bonds. Alkane functional group with examples chemistry page. Initially, lowmolecular, gaseous compounds are predominantly formed which are subsequently transformed again into highermolecular, liquid compounds by an alkylation process called reforming. There are several types of hydrocarbons formed in this reaction and the products include. Oil fractions cracking, isomerisation, reforming 1. Oct 05, 2011 what marine recruits go through in boot camp earning the title making marines on parris island duration. For instance, in both thermal cracking and acidcatalyzed cracking, a monomolecularascission rule is wellknown and generally accounts for most of the ccbond cracking.
Basically, the above reactions are representative only for thermal cracking, i. This is achieved by using high pressures and temperatures without a catalyst, or lower temperatures and pressures in the presence of a catalyst. Catalytic cracking an overview sciencedirect topics. Cracking produces molecules like ethene and propene which are very useful in the organic chemical industry.
Chemical reactions of alkanes chemistry assignment. Cracking is the name given to breaking up large hydrocarbon molecules into. The alkanes range in complexity from the simplest case of methane. Year 12 lesson graded outstanding to teach cracking. You can find instructions for this experiment at liquid paraffin. These ideas are used in df to help learners understand cracking of alkanes to form alkenes, and the reverse reaction in which alkenes are reduced to alkanes. Heres what you need to know about the branched alkanes. This statement is about the use of cracking to make smaller and more useful hydrocarbons from larger hydrocarbons. Combustion reactions the combustion of carbon compounds, especially hydrocarbons, has been the most important source of heat energy for human civilizations throughout recorded history. Cracking, in petroleum refining, the process by which heavy hydrocarbon. We look at how larger alkane molecules are cracked.
Alkanes are saturated hydrocarbons, which means that their carbon backbones contain no double or triple bonds. The hydrocarbons with the lowest boiling points dont condense, theyre drawn off as gases at the top of the column. The chemistry of cracking results in the formation of smaller, more useful alkanes such as petrol, and even more useful alkenes such as ethene. Jul 22, 2017 used for an observation this was aimed for a top set class but can be easily tailored for lower ability students. Which of the following best describes the similarities and differences of compounds, which are isomers. The fractional distillation of crude oil produces alkanes.
Each edge of the chemical structure corresponds to. Useful for assessing your pupils at the end of a topic. Fractional distillation separates different length chains fractions by their boiling points. It is the principal industrial method for producing lighter alkenes olefins, including ethene or ethylene and propene or propylene figure 3. Contains past paper exam style questions and answers.
There are two good economic reasons for cracking oil fractions i there isn. Nomenclature of organic chemistry 1979 and clarified in a guide to iupac nomenclature of organic compounds recommendations 1993. The kinetics of alkane cracking in zeolites mfi and fau have been simulated theoretically from first principles. However, in the case of short alkane molecules like the ones with 8 carbon molecules, they are used extensively in industry as a chemical as well as a fuel, so their demand exceeds their supply. Simply put, hydrocarbon cracking is the process of breaking a longchain of hydrocarbons into short ones. This experimental setup allows operation conditions temperature. However, the longer the carbon chain, the lesser its value, so its usually gets cracked with the cracking process. Cracking is a very important process used in the petrochemical industry to break down the large hydrocarbons intro smaller hydrocarbons, which burns more easily as fuel. You can find instructions for this experiment at resourceres00000681crackinghydrocarbons liquid paraffin. The current theory explaining catalytical cracking is based on ion theory assuming a carbocation intermediate.
Hence, alkanes are quit less reactive and are known as paraffins parumlittle affinisreactivity or affinity. Sep 12, 2017 for these alkanes compound usually set in a solid form are used as wax or candles. This means that they have similar chemical properties to each other and they have trends in physical properties. Petrol and other fuels are produced from it using fractional distillation. Taking a look at ethane and pentane, these alkanes are referred to as saturated because they only contain single bonds, and because of that. In other words, an alkane consists of hydrogen and carbon atoms arranged in a tree structure in which all the carboncarbon bonds are single. In addition to alkanes, cracking reactions may also involve alkenes, alkynes and aromatics. An alkyl group is a group of carbon and hydrogen atoms attached to an alkane molecule. Alkanes and alkenes flashcards in a level and ib chemistry.
Cc bonds break in a way so one electron from a pair goes to each carbon atom, there are not enough hydrogens to produce two alkanes, so an alkene is produced 17 of 60. The mechanism of catalytic cracking has not been fully resolved. There are three types of chemical structure of alkanes known such as linear, branched, and cyclic alkanes. New aqa 2016 gcse chemistry organic lesson 4 and 5. Delivery guide for ocr asa level chemistry b salters. They are hydrocarbons and only consist of single bonds. Combustionsubstitution reactionscatalytic or thermal cracking combustionthe alkanes burn in a plentiful supply of oxygen to produce co2 and h2o. Theoretical simulation of nalkane cracking on zeolites the. Therefore, alkanes are relatively inert with regard to most chemical reagents. Unsaturated hydrocarbons alkenes and alkynes react with h 2 in the presence of finely divided catalysts such as platinum, palladium or nickel to form alkanes. Catalytic cracking of hydrocarbons has long reached technological maturity with only little. Cracking is the process whereby long and medium chain hydrocarbons are heated and break apart giving short chain alkanes, alkenes and hydrogen.
In the petrochemical industry, cracking is part of the refinery process and as such is used to increase the yield of usable alkanes from crude oil. A microscale experiment, cracking the hydrocarbons in paraffin to form shorter alkanes and alkenes. The complex alkanes with high molecular weights that are found in crude oil are frequently broken into smaller, more useful alkanes by thermal cracking. Alkanes are also called as saturated hydrocarbon which includes monocyclic or polycylic molecule. This illustration shows examples of the chemical structures of two alkanes.
The rate of cracking and the end products are strongly dependent on the temperature and presence of catalysts. Thus, the typical reactions of alkanes a1 substitution reactions. The catalytic cracking of alkanes in the presence of deactivation by coke. C 4c 6 alkanes may be heated with platinum or aluminum oxide catalysts to cause isomerism to produce branched chain alkanes. For the love of physics walter lewin may 16, 2011 duration. The alkanes are a homologous series of hydrocarbons.
Lesson planpowerpoint to teach cracking of alkanes. Alkane is solid, liquid or gas at room temperature depends on the size of its molecules. The chemical structure of alkanes only consists of single bonds. In organic chemistry, an alkane, or paraffin a historical name that also has other meanings, is an acyclic saturated hydrocarbon. Apr, 2018 for the love of physics walter lewin may 16, 2011 duration. Cracking produces the smaller hydrocarbons which make up petrol gasoline. Plastic products, gasoline, natural gas alkanes are necessary for us to have these.
Alkanes are chemical compounds that play a very important role in our lives. Discuss both catalytic cracking and thermal cracking of a petroleum fraction. Crude oil is a mixture of different hydrocarbons from organic material buried in the earth and compressed. In petrochemistry, petroleum geology and organic chemistry, cracking is the process whereby complex organic molecules such as kerogens or longchain hydrocarbons are broken down into simpler molecules such as light hydrocarbons, by the breaking of carboncarbon bonds in the precursors. The zeolites used in catalytic cracking are chosen to give high percentages of hydrocarbons with between 5 and 10 carbon atoms particularly useful for petrol gasoline. Questions on sheet at the end of the practical extension. The above situation shows that the development of the petroleum industry is very important for the development of the national economy and organic chemistry. To provide more of the smaller alkane molecules which are in higher demand e.
Fractions rise until they meet a tray just below their boiling point. A fundamental kinetic model for the catalytic cracking of alkanes. The combustion of alkanes, including incomplete combustion. There isnt enough economic use for the larger hydrocarbons. Covers thermal and catalytic cracking, ppt file, application questions, answers and an assessed homework activity with mark scheme. Alkane being saturated compounds can undergo only substitution reactions. The following are some examples for branched alkanes.
Alkanes are used in a number of industrial applications and are found in natural gas. But if undertaken using traditional methods, this practical can lead to the dreaded suckback should students heat for too long or forget to remove the delivery tube from the water at the end of the experiment. A branched chain alkane or branched alkane is an alkane which has alkyl groups bonded to its central carbon chain. Identify the different type of hydrocarbon produced in a high percentage by the thermal cracking of alkanes. In addition to alkanes, cracking reactions may also involve. The difference is that this time you need a catalyst to help break apart the alkanes. Thermal cracking is typically performed at high temperatures, and often in the presence of a catalyst. The cracking of heavy hydrocarbons is one of the fundamental processes in the petrochemical industry. Thermo cracking is used to break down high molecular mass alkanes into low molecular mass alkanes as well as alkenes using heat and a catalyst. Draw the covalent bonding in ethene homework also provided next lesson cracking experiment starter.
Process by which longer chain alkanes are borken down into more commercially viable short chain alkanes and alkenes. Outline of practical work is included but follow centre basedcleaps safety guidelines. The most important reaction of alkanes is combustion reactions, substitution and cracking cracking. Linear alkanes should have the carbons bonded together in a chainlike structure, which is similar to a snake.
In your answer you should quote the conditions used for both cases. It is also known as paraffins or saturated hydrocarbons because carbon and hydrogen atoms are linked together exclusively by single bonds. Learn vocabulary, terms, and more with flashcards, games, and other study tools. Branched alkanes can form linear alkanes but instead of having just a straight chain in their chemical structure, and branched with one or more alkyl groups. Cracking produces the smaller hydrocarbons which make up. Cracking is a thermal decomposition process by which large alkane hydrocarbon molecules are broken down by passing them over a heated catalyst at high pressure.
Identify the products formed and state their uses for both cases. Jul 29, 2019 the process of cracking breaks longer chains alkanes into smaller alkanes and alkenes to increase octane number and to make polymers. Alkanes are generally in towards acids, bases, oxidizing and reducing agents. For each of the following reactions, draw a structural formula equation. Cracking is the name given to breaking up large hydrocarbon molecules. Cracking long chain hydrocarbons into shorter alkanes and alkenes is a staple of the classroom. As chemistry aqa cracking alkanes teaching resources. What marine recruits go through in boot camp earning the title making marines on parris island duration. Alkanes are compounds that consist only carbon and hydrogen, it is a hydrocarbon. Organic chemistry alkanes and alkenes melting point.
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