Concept explainers
(a)
Interpretation:
The structural formula of 4-nitrophenylacetic acid should be drawn.
Concept Introduction:
One of the hydrogen of acetic acid is replaced by para-nitrophenyl group.
(b)
Interpretation:
The structural formula of 4-aminobutanoic acid should be drawn.
Concept Introduction:
One of the hydrogen of butanoic acid is replaced by
(c)
Interpretation:
The structural formula of 4-phenylbutanoic acid should be drawn.
Concept Introduction:
One of the hydrogen of butanoic acid is replaced by phenyl group.
(d)
Interpretation:
The structural formula of cis- 3-hexenedioic acid should be drawn.
Concept Introduction:
Cis compounds are those in which similar groups are on the same side of the double bonds.
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Introduction to General, Organic and Biochemistry
- The SN 1 mechanism starts with the rate-determining step which is the dissociation of the alkyl halide into a carbocation and a halide ion. The next step is the rapid reaction of the carbocation intermediate with the nucleophile; this step completes the nucleophilic substitution stage. The step that follows the nucleophilic substitution is a fast acid-base reaction. The nucleophile now acts as a base to remove the proton from the oxonium ion from the previous step, to give the observed product. Draw a curved arrow mechanism for the reaction, adding steps as necessary. Be sure to include all nonzero formal charges. Cl: Add/Remove step G Click and drag to start drawing a structure.arrow_forwardPlease correct answer and don't use hand ratingarrow_forwardA monochromatic light with a wavelength of 2.5x10-7m strikes a grating containing 10,000 slits/cm. Determine the angular positions of the second-order bright line.arrow_forward
- Curved arrows are used to illustrate the flow of electrons. Us the reaction conditions provided and follow the curved arrow to draw the resulting structure(s). Include all lone pairs and charges as appropriate. H :I H 0arrow_forwardPlease correct answer and don't use hand ratingarrow_forwardNonearrow_forward
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