Rank the following groups in order of decreasing priority?

a.-COOH,-H,-NH2,-OH

b.-CH2CH3,-CH3,-H,-CH(CH3)2

c.-H,-CH3,-Cl,-CH2Cl

d.-CH=CH2,CH3,C≡CH,-H

Short Answer

Expert verified

a. -OH>-NH2>-COOH>-H

b. -CH(CH3)2>-CH2CH3>-CH3>-H

c. -Cl>-CH2Cl>-CH3>-H

d.-C≡CH>-CH=CH2>-CH3>-H

Step by step solution

01

Highest priority groups

The molecules containing atoms or ions of high molecular masses are placed at the first priority. The order of the priority of some groups is:

H<C<O<F<Cl<Br<I

The double bonded groups are multiplied by the same group on the place of a bond.

02

Explanation

a. The order of priority is shown as:

-OH>-NH2>-COOH>-H

The order of the highest priority follows as:

H<C<N<O

Therefore, -OH has the highest priority and H has the lowest priority.

b. The order of priority is shown as:

-CH(CH3)2>-CH2CH3>-CH3>-H

The order of the highest priority follows as:

H<C

Therefore, -CH(CH3)2has the highest priority (highest molecular mass) and H has the lowest priority.

c. The order of priority is shown as:

-Cl>-CH2Cl>-CH3>-H

The order of the highest priority follows as:

H<C<Cl

Therefore, Cl has the highest priority (highest molecular mass), and H has the lowest priority.

d. The order of priority is shown as:

-C≡CH>-CH=CH2>-CH3>-H

The order of the highest priority follows as:

H<C<C=C<C≡C

Therefore, C≡CHhas the highest priority (the triple bond triples each carbon in the molecule) and H has the lowest priority.

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Most popular questions from this chapter

A limited number of chiral compounds having no stereogenic centers exist. For example, although A is achiral, constitutional isomer B is chiral. Make models and explain this observation. Compounds containing two double bonds that share a single carbon atom are called allenes. Locate the allene in the antibiotic mycomycin and decide whether mycomycin is chiral or achiral.

HC≡C-C≡C-CH=C=CH-CH=CH-CH=CH-CH2CO2H

Draw the structures for each compound.

  1. (R)-3-methylhexane
  2. (4R,5S)-4,5-diethyloctane
  3. (3R,5S,6R)-5-ethyl-3,6-dimethylnonane
  4. (3S,6S)-6-isopropyl-3-methyldecane

Give the IUPAC name for each compound, including the R,S designation for each stereogenic center.

a.

b.

c.

A sulfonium ion (R3S+) is a stereogenic center if three different alkyl groups are bonded to sulfur because sulfur is surrounded by four different groups, including its lone pair. In assigning an R or S designation to sulfur, the lone pair is always assigned the lowest priority (4). SAM, S-adenosylmethionine, is a biologically active sulfonium ion that we will learn about in Section 7.16. Locate all the stereogenic centers in SAM, and assign an R,S designation to each center.

Compare the physical properties of the three stereoisomers of 1,3-dimethylcyclopenatane.

  1. How do the boiling points of A and B compare? What about A and C?
  2. Characterize a solution of each of the following as optically active or optically inactive: pure A; pure B; pure C; an equal mixture of A and B; an equal mixture of A and C.
  3. A reaction forms a 1:1:1 mixture of A, B, and C. If this mixture is distilled, how many fractions would be obtained? Which fractions would be optically active and which would be optically inactive?
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