Q1. Write the uses of ethanol.
Answer
Ethanol being a good solvent, it is used in medicines such as tincture iodine (solution of iodine and ethanol), cough mixture and also in many tonics.
Updated on: 2026-03-31 | Author: Rahul Patil
Ethanol being a good solvent, it is used in medicines such as tincture iodine (solution of iodine and ethanol), cough mixture and also in many tonics.
Colorless ethanol is in liquid state at room temperature- Right
Propane is one of the combustible components of L.P.G.
Explanation:
LPG (Liquefied Petroleum Gas) mainly contains propane C3H8 and butane C4H10, which are highly flammable and used as fuels for cooking and heating. Methane and ethane are found in natural gas, while butanol is an alcohol, not a major LPG component.
As one ascends in any homologous series, physical properties change gradually- Right
At room temperature ethanol is liquid.
Benzene is a cyclic unsaturated hydrocarbon- Right
Carbon compounds contain only open chains of carbon atoms- Wrong
CH3–CH2–CHO : propanal : : CH3–COOH : ethanoic acid
| Boiling point of ethanol | → | 78 °C |
| General name of ethanol | → | Ethyl alcohol or spirit |
| Use of ethanol | → | As a solvent in medicines |
| Boiling point of ethanoic acid | → | 118 °C |
| Melting point of pure ethanoic acid | → | 17 °C |
| Straight chain hydrocarbons | Branched chain hydrocarbons | Cyclic hydrocarbons |
| Propane | Isobutylene | Cyclohexane |
| Propyne | Isobutane | Cyclohexene |
| Propene | Cyclopentane | |
| Benzene |
| Name | Molecular formula | Condensed structural formula | Number of carbon atom | Number of -CH2- units | Boiling point °C |
| Methanol | CH4O | CH3-OH | 1 | 1 | 63 |
| Ethanol | C2H6O | CH3–CH2-OH | 2 | 2 | 78 |
| Propanol | C3H8O | CH3–CH2–CH2-OH | 3 | 3 | 97 |
| Butanol | C4H10O | CH3–CH2–CH2–CH2–OH | 4 | 4 | 118 |
| Name | Molecular formula | Condensed structural formula | Number of carbon atom | Number of -CH2- units | Boiling point °C |
| Methane | CH4 | CH4 | 1 | 1 | -162 |
| Ethane | C2H6 | CH3–CH3 | 2 | 2 | -88.5 |
| Propane | C3H8 | CH3–CH2–CH3 | 3 | 3 | -42 |
| Butane | C4H10 | CH3–CH2–CH2–CH3 | 4 | 4 | 0 |
| Pentane | C5H12 | CH3–CH2–CH2–CH2–CH3 | 5 | 5 | 36 |
| Hexane | C6H14 | CH3–CH2–CH2–CH2–CH2–CH3 | 6 | 6 | 69 |
| Name | Molecular formula | Condensed structural formula | Number of carbon atom | Number of -CH2- units | Boiling point °C |
| Ethene | C2H4 | CH2 = CH2 | 2 | 0 | -102 |
| Propene | C3H6 | CH3–CH = CH2 | 3 | 1 | -48 |
| 1-Butene | C4H8 | CH3–CH2–CH = CH2 | 4 | 2 | -6.5 |
| 1-Pentene | C5H10 | CH3–CH2–CH2–CH = CH2 | 5 | 3 | 30 |
| Straight chain of carbon atoms | Structural formula | Molecular formula | Name |
| C-C | \[\begin{array}{cc}\ce{H}\phantom{...}\ce{H}\\ |\phantom{....}|\\\ce{H - C - C - H}\\ |\phantom{....}|\\\ce{H}\phantom{...}\ce{H} \end{array}\] |
C2H6 | Ethane |
| C-C-C-C | \[\begin{array}{cc} \ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\\ |\phantom{....}|\phantom{....}|\phantom{....}|\\\ce{H - C - C - C - C - H}\\|\phantom{....}|\phantom{....}|\phantom{....}|\\ \ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H} \end{array}\] |
C4H10 | Butane |
| C-C-C-C-C-C-C- | \[\begin{array}{cc} \ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\\ |\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\\ \ce{H - C - C - C - C - C - C - C - H}\\ |\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\\ \ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\end{array}\] |
C7H16 | Heptane |
| C-C-C-C-C-C-C-C | \[\begin{array}{cc} \ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\\ |\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\\\ce{H - C - C - C - C - C - C - C - C - H}\\ |\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\\\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H} \end{array}\] |
C8H18 | Octane |
| Sr. No. | Common name | Structural formula | IUPAC Name |
| 1. | ethylene | CH2 = CH2 | Ethene |
| 2. | acetylene | HC ≡ CH | Ethyne |
| 3. | acetic acid | CH3 - COOH | Ethanoic acid |
| 4. | methyl alcohol | CH3 - OH | Methanol |
| 5. | ethyl alcohol | CH3 - CH2 - OH | Ethanol |
| 6. | acetaldehyde | CH3 - CHO | Ethanal |
| 7. | acetone | CH3 - CO - CH3 | Propanone |
| 8. | ethyl methyl ketone | CH3 - CO - CH2 - CH3 | Butanone |
| 9. | ethyl amine | CH3 - CH2 - NH2 | Ethanamine |
| 10. | n-propyl chloride | CH3 - CH2 - CH2 - Cl | 1-Chloropropane |
| Alcohol | -O-H |
| Aldehyde | \[\begin{array}{cc} \ce{O}\phantom{..}\\ ||\phantom{..}\\ \ce{-C-H} \end{array}\] |
| Ketone | \[\begin{array}{cc} \ce{O}\\ ||\\ \ce{-C-} \end{array}\] |
| Carboxylic acid |
\[\begin{array}{cc} \ce{O}\phantom{.....}\\ ||\phantom{.....}\\ \ce{-C-O-H} \end{array}\] |
| Ether | -O- |
| Ester | \[\begin{array}{cc} \ce{O}\phantom{..}\\ ||\phantom{..}\\ \ce{-C-O} \end{array}\] |
| Amine |
\[\begin{array}{cc} |
Cyclohexane : Cyclic hydrocarbon : : Isobutylene : Branched hydrocarbon
Cyclohexane is a branched chain type of hydrocarbon- Wrong
| Alkane | Alkene | |
| 1. | Alkanes are saturated hydrocarbons. | Alkenes are unsaturated hydrocarbons. |
| 2. | They have C−C single bonds. | They have at least one C=C double bond. |
| 3. | They are characterized by the general formula is CnH2n+2. | They are characterized by the general formula is CnH2n. |
| 4. | First member of homologous series is methane. | First member of homologous series is ethene. |
| Open chain hydrocarbons | Closed chain hydrocarbons | |
| 1. | In open chain hydrocarbons, carbon atoms are linked to form a continuous straight or branched chain. | In closed chain hydrocarbons, carbon atoms are linked to form a ring structure. |
| 2. | They are not aromatic compounds. | They can be aromatic compounds. |
| 3. | E.g. Propane, Isobutane | E.g. Cyclohexane, Benzene |
| Saturated hydrocarbons | Unsaturated hydrocarbons | |
| 1. | Hydrocarbons having the carbon atoms linked to each other by single bonds are called saturated hydrocarbons. | Hydrocarbons having at least one carbon-carbon double or triple bond are called unsaturated hydrocarbons. |
| 2. | On burning, saturated hydrocarbons give a clean, blue flame. | On burning, unsaturated hydrocarbons give a yellow flame with lots of black smoke. |
| 3. | Saturated hydrocarbons do not decolourize bromine or iodine solutions. | Unsaturated hydrocarbons decolourize bromine or iodine solutions. |
| 4. | Saturated hydrocarbons are less reactive. | Unsaturated hydrocarbons are usually highly reactive. |
Ester is a sweet-smelling compound- Right
Ethanol is soluble in water in all proportions- Right
Carbon has a unique ability to form strong covalent bonds with other carbon atoms; this results in the formation of big molecules. This property of carbon is called catenation power.
Due to the catenation power of carbon, the compounds formed may have long straight chains of carbon, branched chains of carbon or rings of carbon.
Many carbon compounds are formed in which atoms of elements such as oxygen, nitrogen, sulphur, halogens, etc., substitute one or more hydrogen atoms in the hydrocarbon chain.
The atom of an element other than carbon and hydrogen which replaces one or more hydrogen atoms in the hydrocarbon chain is called a heteroatom.
E.g. In CH3OH, the functional group contains hetero atom ‘O’.
In CH3CH2Cl, the functional group contains hetero atom ‘Cl’.
The reaction in which replacement of an atom or a group of atoms in a molecule by another atom or group of atoms takes place is called substitution reaction. The substitution reactions of alkanes with chlorine occur in presence of sunlight in which one or more hydrogen atoms of alkanes such as methane are replaced by chlorine atoms.
E.g. \[\ce{CH4 + Cl2 ->[Sunlight] CH3Cl + HCl}\]
The reaction in which the addition of a substance occurs across the carbon-carbon double or triple bond is called an addition reaction. Addition reactions occur in unsaturated hydrocarbons.
e.g.
\[\begin{array}{cc}
\phantom{................................}\ce{H}\phantom{...}\ce{H}\\
\phantom{................................}|\phantom{....}|\\
|\phantom{.....}|\phantom{..........................}|\phantom{....}|\\
\ce{\phantom{.}\underset{\text{Ethene}}{H \phantom{...}H}}\phantom{.........................}
\ce{\underset{\text{Ethane}}{H \phantom{...}H}}
\end{array}\]
A chemical reaction in which a substance gains hydrogen or loses oxygen is called a reduction reaction.
E.g. In the following reaction, ethylene (ethene) is reduced to ethane.
Ozone
Explanation-
Ozone is inorganic while others are organic compounds.
C2H2
Explanation-
Ethyne (C2H2) is a unsaturated hydrocarbon while others are saturated hydrocarbons.
C2H4
Explanation-
Ethene (C2H4) is a unsaturated hydrocarbon while others are saturated hydrocarbons.
CaCO3
Explanation-
Calcium carbonate (CaCO3) is an inorganic compound while others are organic compounds.
Teflon
Explanation-
Teflon is a polymer while others are monomer units of respective polymers.
From the following hydrocarbon benzene is the cyclic hydrocarbon.
Generally ethanol is called spirit.
Generally, the melting and boiling point of carbon compounds are found to be less than 300 °C.
E.g. In the hydrogenation of ethene, nickel or platinum is used as catalyst.
\[\begin{array}{cc}
\phantom{................................}\ce{H}\phantom{...}\ce{H}\\
\phantom{................................}|\phantom{....}|\\
|\phantom{.....}|\phantom{..........................}|\phantom{....}|\\
\ce{\phantom{.}\underset{\text{Ethene}}{H \phantom{...}H}}\phantom{.........................}
\ce{\underset{\text{Ethane}}{H \phantom{...}H}}
\end{array}\]
In general, saturated compounds are more reactive than unsaturated compounds- Wrong
The statement is Right.
Explanation:
Liquefied Petroleum Gas (LPG) contains combustible butane and propane. Both extremely combustible gases are used as fuel in homes and factories.
Ketone : –CO– : : Ester : –COO–
| Group 'A' | Group 'B' |
| a. C2H6 | 1. Saturated hydrocarbon |
| b. C2H2 | 2. Triple bond |
| c. CH4O | 3. Molecular formula of an alcohol |
| d. C3H6 | 4. Unsaturated hydrocarbon |
| Group A | Group B |
| 1) Ether | b) –O– |
| 2) Ketone | c) –CO– |
| 3) Ester | d) –COO |
| 4) Alcohol | a) –OH |
| Group A | Group B |
| 1. Straight chain hydrocarbon | b) Propyne |
| 2. Branched chain hydrocarbon | c) Isobutylene |
| 3. Cyclic hydrocarbon | a) Benzene |
Number of valence electrons in a carbon atom is 4.
The reaction shown in the figure is esterification.
Balanced equation of the reaction between ethanol and ethanoic acid is as follows:
\[\ce{\underset{\text{Ethanol}}{C2H5OH} + \underset{\text{Ethanoic acid}}{CH3COOH} ->[Conc.][H2SO4] \underset{\text{Ethyl ethanoate}}{CH3COOC2H5} + \underset{\text{Water}}{H2O}}\]
The product formed is ethyl ethanoate.
Use: It is used for making fragrances and flavouring agents.
The catalyst used in the reaction is concentrated sulphuric acid.
The given hydrocarbon is benzene.
The given hydrocarbon is included in cyclic hydrocarbon.
The compounds having this characteristic unit in their structure are called aromatic compounds.
Potassium permanganate is an oxidizing compound in regular use- Right
Saturated carbon compounds : blue flame : : Unsaturated carbon compounds : Yellow flame
Saturated hydrocarbon : Single bond : : Unsaturated hydrocarbon : Double and/or triple bond
Solid : iodine : : liquid : bromine
The statement is Wrong.
Explanation:
Oxidising agents, not reductants, provide oxygen. A reductant provides electrons to another chemical, reducing it while oxidising the reductant.
The bond between two oxygen atoms is double bond .
The molecular masses of a carbon compound spread over a range of 1012.
The number of electrons in the valence shell of a carbon atom is 4- Right
The unsaturated hydrocarbons containing a carbon-carbon double bond are called Alkenes.
This statement is Wrong.
Catalyst is a substance which increases the rate of a reaction without causing any disturbance to it.
An oxidising agent is a reactant which readily transfers oxygen atoms to another substance by reducing itself in the process.
While going in an increasing order there is a rise in the molecular mass of the consecutive members of the homologous series by 14 u.
The unique property of carbon atom to form covalent bonds with other carbon atoms giving rise to extremely big molecules is called catenation power.
The covalent bond between two carbon atoms is strong and stable.
This is the reason carbon is bestowed with catenation power.
Due to catenation power, carbon can form a large number of compounds containing open chains or closed chains of carbon atoms.
Catenation power: Carbon has a unique ability to form strong covalent bonds with other carbon atoms; this results in the formation of big molecules. This property of carbon is called catenation power.
Multiple bond formation: Two carbon atoms can be bonded together by one, two or three covalent bonds. These are called a single bond, double bond, and triple bond respectively. Thus, carbon atom has the ability to form multiple bonds as well as single bonds.
Tetravalency: Being tetravalent one carbon atom can form bonds with four other atoms (carbon or any other). This results in formation of many compounds.
Isomerism: One more characteristic of carbon, which is responsible for large number of carbon compounds is isomerism.
Many more types of carbon compounds are formed by formation of bonds of carbon with other elements such as halogens, oxygen, nitrogen, sulphur.
The atoms of these elements (hetero atoms) substitute one or more hydrogen atoms in the hydrocarbon chain and thereby the tetravalency of carbon is satisfied.
The compound acquire specific chemical properties due to these heteroatoms or the groups of atoms that contain heteroatoms, irrespective of the length and nature of the carbon chain in that compound.
E.g. In CH3 – OH, –OH (alcohol) is the functional group-containing heteroatom ‘oxygen’.
The series of carbon compounds formed by joining the same functional group in the place of a particular hydrogen atom on the carbon chains having sequentially increasing length is called homologous series.
There are different homologous series in accordance with the functional group. For example, homologous series of alcohols, homologous series of carboxylic acids, homologous series of aldehydes, etc.
Physical properties generally show a gradual change with the increase in molecular mass in the series whereas chemical properties of the members of the series show similarity because of the presence of the same functional group in them.
The saturated hydrocarbons containing only single bonds between carbon atoms are called alkanes.
An alkene is an unsaturated hydrocarbon that contains at least one carbon-carbon double bond.
An alkyne is a type of unsaturated hydrocarbon characterized by the presence of at least one carbon-carbon triple bond.
Vinegar is the type of liquid which consist of acetic acid ( Ethanoic acid ). It is basically produced by the process of fermentation of ethanol through ethanoic acid in the presence of bacteria.
Reaction involved in the formation of Vinegar:
CH₃CH₂OH + O₂ → CH₃COOH + H₂O
Fermentation is the process of converting sugar into alcohol. But if the cork of the bottle open for sometimes then there is a second type of fermentation happened. In this process, alcohol is changes into acetic acid, so the main compound which formed is vinegar.
Uses of Vinegar are:
It is used in the preparation of the food.
It is used in pickling.
It is used as folk medicine material.
It is used as a household cleaning agent
Gasohol is a mixture of 90% gasoline and 10% of anhydrous Alcohol (Ethyl Alcohol). It is commonly known as alternative fuel or motor fuel.
Benefits of gasohol are:-
It is cheaper.
It is eco-friendly.
It has higher performance.
It is used as a cleaner for the environment.
It doesn't freeze in typical conditions.
Uses of gasohol are:
It is used in a fuel or petroleum Industry
It is used in an automobiles industry
It is used as common gasoline or hydrous around the world.
It is used as a flexible fuel vehicle, because it do not freeze in typical conditions.
Benzene compounds are cyclic unsaturated hydrocarbons having structure similar to benzene.
There are three alternate double bonds in the six-membered ring structure of benzene.
Compounds having this characteristic unit in their structures are called aromatic compounds.
Carbon is a tetravalent atom with the property of catenation. Thus, it forms compounds in which the carbon atoms are arranged in the form of straight chains, branched chains or rings.
It can form single and multiple covalent bonds with other carbon atoms.
Carbon is tetravalent. Thus, it can form four covalent bonds with carbon or other elements like oxygen, nitrogen, sulphur, halogens and phosphorus.
One more characteristics of carbon, which is responsible for large number of carbon compounds is isomerism.
Hydrocarbons containing at least one carbon-carbon double or triple bond are called unsaturated hydrocarbons.
Vegetable oils are unsaturated fatty acids.
They contain carbon-carbon multiple bonds and thus, undergo addition reaction with iodine.
Naphthalene is an unsaturated hydrocarbon.
Unsaturated hydrocarbons burns with a yellow flame and releases black soot/smoke.
Vegetable oil contains carbon-carbon multiple bonds while vanaspati ghee contains carbon-carbon single bonds. So, vegetable oil is an unsatured compound while vanaspati ghee is a saturated compound.
An unsaturated compound undergoes addition reaction with hydrogen in presence of nickel catalyst to form a saturated compound. This reaction is called hydrogenation.
Balanced equation of the reaction between acetic acid and sodium carbonate is as follows:
\[\ce{\underset{\text{Acetic acid}}{2CH3COOH_{(aq)}} + \underset{\text{carbonate}}{\underset{\text{Sodium}}{Na2CO_{3(s)}}} -> \underset{\text{ethanoate}}{\underset{\text{Sodium}}{2CH3COONa_{(aq)}}} + \underset{\text{Water}}{H2O_{(l)}} + \underset{\text{Carbon dioxide}}{CO2\uparrow}}\]
The gas formed in the large test tube is carbon dioxide (CO2) gas.
Lime water turns milky.
Ethanoic acid is a colourless liquid at ordinary temperature.
Its boiling point is 118 °C.
Melting point of pure ethanoic acid is 17 °C.
It is colourless liquid at room temperature and
Its boiling point is 78 °C.
It is soluble in water in all proportions.
Its aqueous solution is neutral.
Acetic acid- CH3COOH or C2H4O2
Acetone- C3H6O
Acetylene- C2H2
Benzene- C6H6
Ethanoic acid- CH3COOH or C2H4O2
Ethanol- C2H5OH or C2H6O
Ethyl alcohol- C2H5OH or C2H6O
Ethyl ethanoate- C4H8O2
Ethylene- C2H4
Isobutane- C4H10
Oleic acid- C17H33COOH or C18H34O2
Palmitic acid- C15H31COOH or C16H32O2
Propene- C3H6
Propylene- C3H6
Sodium ethanoate- C2H3O2Na
Sodium ethoxide- C2H5ONa
Stearic acid- C17H35COOH or C18H36O2
| \[\begin{array}{cc}\phantom{......}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{..}\\ \phantom{.....}|\phantom{....}|\phantom{....}|\\ \ce{H - C - C = C}\\\phantom{.....}|\phantom{.........}|\\ \phantom{.....}\ce{H}\phantom{........}\ce{H}\end{array}\] |
Propene |
| \[\begin{array}{cc}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\\ |\phantom{....}|\phantom{....}|\\\ce{H - C - C - C - H}\\ |\phantom{....}|\phantom{....}|\\\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H} \end{array}\] |
Propane |
| \[\begin{array}{cc} \phantom{.........}\ce{H}\\ \phantom{.........}|\\ \ce{H - C ≡ C - C - H}\\ \phantom{.........}|\\ \phantom{.........}\ce{H} \end{array}\] |
Propyne |
| \[\begin{array}{cc} \phantom{..}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\\ \phantom{..}|\phantom{....}|\phantom{....}|\\ \ce{H - C - C- C- H}\\ \phantom{.}|\phantom{....}|\phantom{....}|\\ \ce{H - C - H}\\ |\\\ce{H}\end{array}\] |
Isobutane |
Your body is made up of carbon- Right