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(a)
Interpretation:
Fischer projection structure of the given molecule is to be drawn.
Concept introduction:
The two-dimensional projection of a three-dimensional organic molecule is nothing but Fischer projection. Fischer projections are generally drawn with the longest carbon chain vertical. The two groups attached to each carbon except the first and last are shown on horizontal bonds. The carbon atoms in the middle of the chain are represented by the intersections of vertical and horizontal lines. The vertical lines show bonds that aligned away from the observer, while the horizontal bonds are aligned towards the observer.
Interpretation:
(b)
Fischer projection of the given molecule is to be drawn.
Concept introduction:
The two-dimensional projection of a three-dimensional organic molecule is nothing but Fischer projection. Fischer projections are generally drawn with the longest carbon chain vertical. The two groups attached to each carbon except the first and last are shown on horizontal bonds. The carbon atoms in the middle of the chain are represented by the intersections of vertical and horizontal lines. The vertical lines show bonds that aligned away from the observer, while the horizontal bonds are aligned towards the observer.
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Chapter 5 Solutions
Organic Chemistry: Principles and Mechanisms (Second Edition)
- The bromination of anisole is an extremely fast reaction. Complete the resonance structures of the intermediate arenium cation for the reaction (Part 1), and then answer the question that follows (Part 2).arrow_forwardDrawing of 3-fluro-2methylphenolarrow_forwardWhich compound(s) will be fully deprotonated (>99%) by reaction with one molar equivalent of sodium hydroxide? I, II, III I, || I, III I only II, III SH | H3C-C=C-H || III NH2arrow_forward
- Will NBS (and heat or light) work for this reaction, or do we have to use Br2?arrow_forwardHAND DRAWarrow_forwardPredict the major products of the following organic reaction: Some important notes: Δ CN ? • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. ONO reaction. Click and drag to start drawing a structure.arrow_forward
- The following product was made from diethyl ketone and what other reagent(s)? £ HO 10 2-pentyne 1-butyne and NaNH2 ☐ 1-propanol ☐ pyridine butanal ☐ pentanoatearrow_forwardWhich pair of reagents will form the given product? OH X + Y a. CH3 b. CH2CH3 ༧་་ C. CH3- CH2CH3 d.o6.(རི॰ e. CH3 OCH2CH3 -MgBr f. CH3-MgBr g. CH3CH2-MgBr -C-CH3 CH2CH3arrow_forwardQuestion 3 What best describes the product of the following reaction? 1. CH3CH2MgBr (2 eq) 2. H a new stereocenter will not be formed a new stereocenter will be formed an alkyl halide will result an alkane will result an aromatic compound will result 1 ptsarrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
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