Maharashtra State Board 11th Chemistry Solutions Chapter 15 Hydrocarbons
1. Choose correct options
Question A.
Which of the following compound has the highest boiling point?
a. n-pentane
b. iso-butane
c. butane
d. neopentane
Answer:
a. n-pentane
Question B.
Acidic hydrogen is present in :
a. acetylene
b. ethane
c. ethylene
d. dimethyl acetylene
Answer:
a. acetylene
Question C.
Identify ‘A’ in the following reaction:
a. KMnO4/H+
b. alkaline KMnO4
c. dil. H2SO4/1% HgSO4
d. NaOH/H2O2
Answer:
a. KMnO4/H+
Question D.
Major product of chlorination of ethyl benzene is :
a. m-chlorethyl benzene
b. p-chloroethyl benzene
c. chlorobenzene
d. o-chloroethylbenzene
Answer:
b. p-chloroethyl benzene
Question E.
1 – chloropropane on treatment with alc. KOH produces :
a. propane
b. propene
c. propyne
d. propyl alcohol
Answer:
b. propene
2. Name the following :
Question A.
The type of hydrocarbon that is used as lubricant.
Answer:
Waxes
Question B.
Alkene used in the manufacture of polythene bags.
Answer:
Ethene
Question C.
The hydrocarbon said to possess carcinogenic property.
Answer:
Benzene
Question D.
What are the main natural sources of alkane?
Answer:
Crude petroleum and natural gas.
Question E.
Arrange the three isomers of alkane with malecular formula C5H12in increasing order of boiling points and write their IUPAC names.
Answer:
The three isomers of alkane with molecular formula C5H12are as follows:
The increasing order of their boiling point is I > II > III.
Question F.
Write IUPAC names of the products obtained by the reaction of cold concentrated sulphuric acid followed by water with the following compounds.
a. propene
b. but-1-ene
Answer:
a. propene:
b. but-1-ene:
Question G.
Write the balanced chemical reaction for preparation of ethane from
a. Ethyl bromide
b. Ethyl magnesium iodide
Answer:
a. Preparation of ethane from ethyl bromide:
b. Preparation of ethane from ethyl magnesium iodide:
Question H.
How many monochlorination products are possible for
a. 2-methylpropane ?
b. 2-methylbutane ?
Draw their structures and write their IUPAC names.
Answer:
a. Possible monochlorination products for 2-methylpropane:
b. Possible monochlorination products for 2-methylbutane:
Question I.
Write all the possible products for pyrolysis of butane.
Answer:
Possible products for pyrolysis of butane are:
Question J.
Which of the following will exhibit geometical isomerism ?
Answer:
Compound (c) will exhibit geometrical isomerism.
Question K.
What is the action of following on ethyl iodide ?
a. alc. KOH
b. Zn, HCl
Answer:
a. Action of alc. KOH on ethyl iodide:
b. Action of Zn/HCl on ethyl iodide:
Question L.
An alkene ‘A’ an ozonolysis gives 2 moles of ethanal. Write the structure and IUPAC name of ‘A’.
Answer:
Structure of A: CH3– CH = CH – CH3
IUPAC name of A: But-2-ene
Question M.
Acetone and acetaldehyde are the ozonolysis products of an alkene. Write the structural formula of an alkene and give IUPAC name of it.
Answer:
The structural formula of alkene:
IUPAC name is 2-methylbut-2-ene.
Question N.
Write the reaction to convert
a. propene to n-propyl alcohol.
b. propene to isoproyl alcohol.
Answer:
a.
b.
Question O.
What is the action of following on but-2-ene ?
a. dil alkaline KMnO4
b. acidic KMnO4
Answer:
a. Action of dil. alkaline KMnO4on but-2-ene:
b. Action of acidic KMnO4on but-2-ene:
Question P.
Complete the following reaction sequence :
Answer:
Question Q.
Write the balanced chemical reactions to get benzene from
a. Sodium benzoate.
b. Phenol.
Answer:
a. Sodium benzoate:
When anhydrous sodium benzoate is heated with soda lime, it undergoes decarboxylation and gives benzene.
b. Phenol:
When vapours of phenol are passed over heated zinc dust, it undergoes reduction and gives benzene.
Question R.
Predict the possible products of the following reaction.
a. chlorination of nitrobenzene,
b. sulfonation of chlorobenzene,
c. bromination of phenol,
d. nitration of toluene.
Answer:
a. Nitro group is meta directing group. So, chlorination of nitrobenzene gives m-chloronitrobenzene.
b. Chloro group is ortho and para directing group. So, sulphonation of chlorobenzene gives p-chlorobenzene sulphonic acid and o- chlorobenzene sulphonic acid.
c. Phenolic -OH group is ortho and para directing group. So, bromination of phenol gives p-bromophenol and o-bromophenol.
d. Methyl group is ortho and para directing group. So, nitration of toluene gives p-nitrotoluene and o-nitrotoluene.
3. Identify the main product of the reaction
Answer:
a.
b.
c.
d.
4. Read the following reaction and answer the questions given below.
a. Write IUPAC name of the product.
b. State the rule that governs formation of this product.
Answer:
a. IUPAC name of the product: 1 -Bromo-2-methylpropane
b. Anti-Markownikov’s rule/Kharasch effect/peroxide effect: It states that, the addition of HBr to unsymmetrical alkene in the presence of organic peroxide (R-O-O-R) takes place in the opposite orientation to that suggested by Markovnikov’s rule.
5. Identify A, B, C in the following reaction sequence :
Answer:
6. Identify giving reason whether the following compounds are aromatic or not.
Answer:
A.
Compound is non-aromatic since it has 4π electrons and hence, does not obey Huckel rule of aromaticity.
B.
Compound is non-aromatic since it has 4π electrons and hence, does not obey Huckel rule of aromaticity.
C.
Compound is aromatic since it has 6π electrons and hence, obeys Huckel rule of aromaticity.
D.
Compound is aromatic since it has 6n electrons and hence, obeys Huckel rule of aromaticity.
7. Name two reagents used for acylation of benzene.
Answer:
The two reagents used for acylation of benzene are:
i. CH3COCl (acetyl chloride) and anhydrous AlCl3
ii. (CH3CO)2O (acetic anhydride) and anhydrous AlCl3
8. Read the following reaction and answer the questions given below.
A. Write the name of the reaction.
B. Identify the electrophile in it.
C. How is this electrophile generated?
Answer:
A. The name of the reaction is Friedel-Craft’s alkylation reaction.
B. The electrophile in the reaction is+CH3.
C. The electrophile+CH3is generated as follows:
Activity:
Prepare chart of hydrocarbons and note down the characteristics.
Answer:
Characteristics of hydrocarbons:
[Note: Students are expected to collect additional information on hydrocarbons on their own.]
11th Chemistry Digest Chapter 15 Hydrocarbons Intext Questions and Answers
Can you recall? (Textbook Page No. 233)
Question i.
What are hydrocarbons?
Answer:
The compounds which contain carbon and hydrogen as the only elements are called hydrocarbons.
Question ii.
Write structural formulae of the following compounds: propane, ethyne, cyclobutane, ethene, benzene.
Answer:
Do you know? (Textbook Page No. 233)
Internet my friend. (Textbook Page No. 233)
[Note: Students are expected to collect additional information on their own]
Use your brain power! (Textbook Page No. 234)
Note:
Alkanes and isomer number
Number of Carbon | Alkane | Number of isomers |
1 | Methane | No structural isomer |
2 | Ethane | No structural isomer |
3 | Propane | No structural isomer |
4 | Butane | Two |
5 | Pentane | Three |
6 | Hexane | Five |
Can you recall? (Textbook Page No. 235)
Question i.
What is a catalyst?
Answer:
A catalyst is a substance that can be added to a reaction to increase the reaction rate without getting consumed in the process.
e.g. Ni is used as a catalyst in the catalytic hydrogenation of alkenes or alkynes.
Question ii.
What is addition reaction?
Answer:
When a compound combines with another compound to form a product that contain all the atoms in both the reactants, it is called an addition reaction.
Try this (Textbook Page No. 235)
Use your brain power! (Textbook Page No. 236)
Hence, alkanes are insoluble in water and readily soluble in organic solvents like chloroform or ether.
Can you recall? (Textbook Page No. 238)
Can you recall? (Textbook Page No. 238)
Question i.
What are alkenes?
Answer:
Alkenes are unsaturated hydrocarbons containing at least one carbon-carbon double bond.
Question ii.
Calculate the number of sigma (σ) and pi (π) bonds in 2-methylpropene.
Answer:
Question iii.
Write the structural formula of pent-2-ene.
Answer:
Can you tell? (Textbook Page No. 241)
Question i.
Explain by writing a reaction, the main product formed on heating 2-methylbutan-2-ol with concentrated sulphuric acid.
Answer:
Question ii.
Will the main product in the above reaction show geometrical isomerism?
Answer:
No, the major product, i.e., 2-methylbut-2-ene does not show geometrical (or cis-trans) isomerism.
Can you tell? (Textbook Page No. 244)
Use your brainpower. (Textbook Page No. 244)
Use your brain power! (Textbook Page No. 245)
Polymer | Monomeric unit | |
i. | Teflon | CF2– CF2Tetrafluoroethene |
ii. | Polypropene | H3C – CH = CH2Propene |
iii. | Polyvinyl chloride | H2C = CHCl |
Can you tell? (Textbook Page No. 246)
Question i.
What are aliphatic hydrocarbons?
Answer:
Aliphatic hydrocarbons are hydrocarbons containing carbon and hydrogen joined together in straight chain or branched chain. They may be saturated (alkanes) or unsaturated (alkenes or alkynes).
Question ii.
Compare the proportion of carbon and hydrogen atoms in ethane, ethene and ethyne. Which compound is most unsaturated with hydrogen?
Answer:
Ethane
C : H = 2 : 6 = 1 : 3
Ethene
C : H = 2 : 4 = 1 : 2
Ethyne
C : H = 2 : 2 = 1 : 1
From the above proportion it is clear that ethyne with 1 : 1 ratio of C : H is most unsaturated with hydrogen (50%) as compared to ethane (25%) and ethene (33.33%).
Can you tell? (Textbook Page No. 247)
Use your brainpower! (Textbook Page No. 247)
Can you tell? (Textbook Page No. 248)
Use your brain power! (Textbook Page No. 248)
Use your brain power! (Textbook Page No. 249)
Can you recall? (Textbook Page No. 249)
Question i.
What are aromatic hydrocarbons?
Answer:
Benzene and all compounds that have structures and chemical properties resembling benzene are called as aromatic hydrocarbons.
Question ii.
What are benzenoid and non-benzenoid aromatics?
Answer:
Benzenoid aromatics are compounds having at least one benzene ring in the structure.
e.g. Benzene, naphthalene, anthracene, phenol, etc.,
Non-benzenoid aromatics are compounds that contain an aromatic ring, other than benzene. e.g. Tropone, etc.
Can you recall? (Textbook Page No. 254)