Alkane 烷烃
Akene 烯烃
Alcohol 醇
Carboxylic acid 羧酸
Ester 酯
100

What is the general formula of alkanes?

A) CnH2n

B) CnH2n+2

C) CnH2n+1

D) CnH2n-2

B

100

 What is the general formula of alkenes?  

A) CnH2n

B) CnH2n+2

C) CnH2n+1

D) CnH2n-2

A

100

Which functional group is present in all alcohols?  

A) -COOH  

B) -OH  

C) -COO-  

D) -Cl  


B) -OH  

100

 What is the functional group of carboxylic acids?  

A) -OH  

B) -COOH  

C) -COO-  

D) -CHO  


B) -COOH  

100

Esters are formed from the reaction between a carboxylic acid and which other compound?  

A) Alkane  

B) Alcohol  

C) Alkene  

D) Halogen  


B) Alcohol  

200

Which type of reaction occurs when methane reacts with chlorine in the presence of UV light?  


A) Addition  

B) Combustion  

C) Substitution  

D) Oxidation  


C

200

Which reagent is used to test for the presence of a carbon-carbon double bond in alkenes?  

A) Sodium hydroxide  

B) Bromine water  

C) Litmus paper  

D) Potassium dichromate  


B) Bromine water  

200

What is the molecular formula of ethanol?  

A) C2H5OH

B) C3H7OH  

C) C2H4O

D) CH3COOH


A) C2H5OH

200

Which gas is produced when ethanoic acid reacts with magnesium?  

A) Carbon dioxide  

B) Hydrogen  

C) Oxygen  

D) Methane  


B) Hydrogen  

200

What is the name of the ester formed when methanol reacts with propanoic acid?  

A) Methyl propanoate  

B) Propyl methanoate  

C) Ethyl ethanoate  

D) Butyl butanoate  


A) Methyl propanoate  

300

Write the balanced equation for the complete combustion of propane in oxygen.  


CH3CH2CH3(g) +5O2(g) → 3CO2(g) + 4H2O(l)


300

An alkene has 8 carbon atoms. Calculate its molecular formula and empirical formula。

molecular formula is C8H18
empirical formula is C4H9

300

Write the balanced equation for the complete combustion of Propanol ( C3H7OH ) in oxygen.  


C3H7OH + 9/2O2→ 3CO2 + 4H2O

300

Write the equation for the reaction between ethanoic acid and sodium carbonate.

2CH3COOH + Na2CO3 → 2CH3COONa + CO2 + H2


300

Write the equation for the reaction between ethanoic acid and ethanol to form an ester.  


CH3COOH + C2H5OH → CH3COOC2H5 + H2


400

Draw the equation when ethane reacts with chlorine in a substitution reaction, including condition (other product is HCl).

CH3CH3(g) +Cl2(g) → CH3CH2Cl(g) + HCl(l)

the reactions of alkanes with halogens in the presence of ultraviolet radiation(UV light)

400

Ethene (C2H4) reacts with bromine in an addition reaction. Draw the displayed structure of the product.  


     H   H  

     |   |  

Br─C─C─Br  

     |   |  

     H   H  


400

Compare the advantages and disadvantages of producing ethanol via fermentation vs the reaction of ethene with steam.  


**Fermentation**: Renewable resources (sugar)
at an optimum temperature of about 30 ºC , but low yield.

**Ethene + steam**: Non-renewable (crude oil), in the presence of a phosphoric acid catalyst at a temperature of about 300 ºC, but high yield.


400

 Draw the structural formula of propanoic acid.  


Structural formula of propanoic acid:  

CH3CH2COOH


400

Explain why esters are used in perfumes and food flavorings?


Esters are volatile and have pleasant, fruity aromas, making them ideal for perfumes and flavorings.  


500

 Explain why alkanes are described as "saturated" hydrocarbons?


Alkanes are saturated because all carbon-carbon bonds are single bonds, allowing each carbon atom to bond with the maximum number of hydrogen atoms.  


500

Explain why alkenes are more reactive than alkanes?

Alkenes are more reactive due to the electron-rich C=C double bond, which can undergo addition reactions.  


500

Explain why the oxidation of ethanol with acidified potassium dichromate(VI) produces ethanoic acid?


Acidified potassium dichromate(VI) oxidizes ethanol’s -OH group to -COOH, forming ethanoic acid.  


500

Explain why carboxylic acids are weaker acids compared to hydrochloric acid?


Carboxylic acids only partially dissociate in water, releasing fewer Hions compared to strong acids like HCl.  


500

Describe the steps to prepare ethyl ethanoate in a laboratory.  


1. Mix ethanoic acid, ethanol, and concentrated  H2SO4 .  

2. Heat in a water bath at 60 0C .  

3. Cool and pour into sodium carbonate solution.  

4. Ester layer forms on top.