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Review 2nd Partial M&S

Total questions: 10

Worksheet time: 20mins

Name
Class
Date
1.

What does Carbon tetravalence mean?

a)

Carbon has valence electrons

b)

Carbon always forms 4 bonds with its 4 valence electrons

c)

Carbon can have up to 4 bonds

2.

In linear formulas, Carbon doesn't have bonds with Hydrogens

a)

true

b)

false

c)

Hydrogens are not represeted but the bonds exist

d)

There are only Carbons in those formulas

3.

This structure can be classified as?

a)

open chain, branched, unsaturated, alkene

b)

open chain, alkene

c)

linear, open chain, unsaturated

d)

aliciclyc, branched, unsaturated

4.

This compound can be classified as

a)

alicyclic, homocyclic, unsaturated, branched

b)

closed chain, aromatic, linear

c)

branched, homocyclic, closed

d)

aromatic, heterocyclic, branched

5.

Carbons that have sp3 hybridization have the following characteristics:

a)

all single bonds, tetrahedral geometry, 109° angles

b)

sigma and pi bonds

c)

sigma bonds, tetrahedral geometry, 120° angles

d)

2 pi bonds and 109° angles

6.

How many sigma and pi bonds are present in this molecule?

a)

11 sigma and 1 pi

b)

10 sigma and 1 pi

c)

2 pi and 11 sigma

d)

10 sp3 bonds

7.

As a hydrocarbon increases in number of C, the boiling point will tend to:

a)

increase

b)

decrease

c)

stay de same

d)

have more Hydrogens

8.

Tyrosine is an aminoacid, which functional groups must be present?

a)

carboxylic acid

b)

carboxylic acid and amine

c)

carboxylic acid and amide

d)

amine and aldehyde (the aldehyde is turned into a carboxylic acid)

9.

A company that produces detergents observed that in the last client solutions panel: customers prefer a wide variety of fruity smells for floor and surfaces detergents. Which of the following companies are they likely to make new business with?

a)

Wade and Co. Esters

b)

International Alcohols S.A. de C.V.

c)

Amines and Amides: your trusted Chemical company

d)

East Coast Hydrocarbons: the best energy solution for your company

10.

When naming an ester you should always include the position of the -yl (R-O) part of the ester.

a)

false

b)

true

c)

you need to include the oate position as well

d)

in only needs the position of the oate part