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(a)
Interpretation:
The following molecule should be named:
Concept Introduction:
Ethers are molecules which have two alkyl groups bonded to the oxygen atom.
Simple ethers named based on their structure.
In ether nomenclature, both alkyl groups are named and arranged them according to the alphabetical order and at the end of the name word 'ether' should be added. Ethers which have identical alkyl groups, prefix di- should be added to the alkyl group.
When naming more complex ethers according to the
(b)
Interpretation:
The following molecule should be named:
Concept Introduction:
Organic compounds which contains a sulfhydryl group (SH) bonded to a tetrahedral carbon is known as thiols. In the periodic table, sulfur is placed directly below to the oxygen, thiols can be considered as sulfur analogs of alcohols.
When naming the thiols, parent hydrocarbon is named as alkane and at the end -thiol suffix should be added. Main carbon chain is numbered by giving the SH group the lower number.
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Chapter 14 Solutions
EBK GENERAL, ORGANIC, & BIOLOGICAL CHEM
- 1. For the four structures provided, Please answer the following questions in the table below. a. Please draw π molecular orbital diagram (use the polygon-and-circle method if appropriate) and fill electrons in each molecular orbital b. Please indicate the number of π electrons c. Please indicate if each molecule provided is anti-aromatic, aromatic, or non- aromatic TT MO diagram Number of π e- Aromaticity Evaluation (X choose one) Non-aromatic Aromatic Anti-aromatic || ||| + IVarrow_forward1.3 grams of pottasium iodide is placed in 100 mL of o.11 mol/L lead nitrate solution. At room temperature, lead iodide has a Ksp of 4.4x10^-9. How many moles of precipitate will form?arrow_forwardQ3: Circle the molecules that are optically active: ДДДДarrow_forward
- 6. How many peaks would be observed for each of the circled protons in the compounds below? 8 pts CH3 CH3 ΤΙ A. H3C-C-C-CH3 I (₁₁ +1)= 7 H CI B. H3C-C-CI H (3+1)=4 H LIH)=2 C. (CH3CH2-C-OH H D. CH3arrow_forwardNonearrow_forwardQ1: Draw the most stable and the least stable Newman projections about the C2-C3 bond for each of the following isomers (A-C). Are the barriers to rotation identical for enantiomers A and B? How about the diastereomers (A versus C or B versus C)? H Br H Br (S) CH3 (R) CH3 H3C (S) H3C H Br Br H A C enantiomers H Br H Br (R) CH3 H3C (R) (S) CH3 H3C H Br Br H B D identicalarrow_forward
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