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grigory [225]
3 years ago
12

Chemistry! Help! Please!! Thanks

Chemistry
1 answer:
Vladimir79 [104]3 years ago
7 0

Answers:

1. 3-ethyl-3-methylheptane; 2. 2,2,3,3-tetramethylpentane; 3. hexa-2,4-diene.

Explanation:

<em>Structure 1 </em>

  1. Identify and name the longest continuous chain of carbon atoms (the main chain has 7 C; ∴ base name = heptane).
  2. Identify and name all the substituents [a 1C substituent (methyl) and a 2C substituent (methyl).
  3. Number the main chain from the end closest to a substituent.
  4. Identify the substituents by the number of the C atom on the main chain. Use hyphens between letters and numbers (3-methyl, 3-ethyl).
  5. Put the names of the substituents in alphabetical order in front of the base name with no spaces (3-ethyl-3-methylheptane)

<em>Structure 2</em>

  1. 5C. Base name = pentane
  2. Four methyl groups.
  3. Number from the left-hand end.
  4. If there is more than one substituent of the same type, identify each substituent by its locating number and use a multiplying prefix to show the number of each substituent. Use commas between numbers (2,2,3,3-tetramethyl).
  5. The name is 2,2,3,3-tetramethylpentane.

<em>Structure 3 </em>

  1. Identify and name the longest continuous chain of carbon atoms that passes through as many double bonds as possible. Drop the <em>-ne</em> ending of the alkane to get the root name <em>hexa-</em>.
  2. (No substituents).
  3. Number the main chain from the end closest to a double bond.
  4. If there is more than one double bond use a multiplying prefix to indicate the number of double bonds (two double bonds = diene) and use the smaller of the two numbers of the C=C atoms as the double bond locators (2,4-diene)
  5. Put the functional group name at the end of the root name (hexa-2,4-diene).

<em>Note</em>: The name 2,4-hexadiene is <em>acceptable</em>, but the <em>Preferred IUPAC Name</em> puts the locating numbers as close as possible in front of the groups they locate.

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