
(a)
Interpretation: Structure of
Concept introduction: In accordance with
As per IUPAC recommendations, longest chain found in a continuous manner in a branched molecule is chosen as parent chain. The longest chain must contain the alcohol functional group.The chain carbons are numbered so as to provide least numeral position towards the end in vicinity to
In
(b)
Interpretation: Structure of
Concept introduction:In accordance with IUPAC systematic nomenclature of alcohols can be derived from the parent alkane with “e” dropped and replaced by “ol” suffix.
As per IUPAC recommendations, longest chain found in a continuous manner in a branched molecule is chosen as parent chain. The longest chain must contain the alcohol functional group.The chain carbons are numbered so as to provide least numeral position towards the end in vicinity to
In alkanes, the positions of side chains or alkyl substituents are indicated by lowest numeral places before prefix.
(c)
Interpretation: Structure of
Concept introduction:In accordance with IUPAC systematic nomenclature of alcohols can be derived from the parent alkane with “e” dropped and replaced by “ol” suffix.
As per IUPAC recommendations, longest chain found in a continuous manner in a branched molecule is chosen as parent chain. The longest chain must contain the alcohol functional group.The chain carbons are numbered so as to provide least numeral position towards the end in vicinity to
In alkanes, the positions of side chains or alkyl substituents are indicated by lowest numeral places before prefix.
In order to assign absolute configuration of R and S, Cahn−Ingold−Prelog rules are used and the first step is to assign the priority order on the basis of
The Fischer projection is written along with the priorities assigned and groups are interchangedbetween adjacent places so as to obtain lowest priority group at the bottom or lowest priority.
If the groups now are arranged are read from highest towards least in clockwise fashion the R is assigned to the stereocenter, if the rotation is anticlockwise the S is assigned at the configuration.
(d)
Interpretation: Structure of
Concept introduction:In accordance with IUPAC systematic nomenclature of alcohols can be derived from the parent alkane with “e” dropped and replaced by “ol” suffix.
As per IUPAC recommendations, longest chain found in a continuous manner in a branched molecule is chosen as parent chain. The longest chain must contain the alcohol functional group.The chain carbons are numbered so as to provide least numeral position towards the end in vicinity to
In alkanes, the positions of side chains or alkyl substituents are indicated by lowest numeral places before prefix.
(e)
Interpretation: Structure of
Concept introduction:In accordance with IUPAC systematic nomenclature of alcohols can be derived from the parent alkane with “e” dropped and replaced by “ol” suffix.
As per IUPAC recommendations, longest chain found in a continuous manner in a branched molecule is chosen as parent chain. The longest chain must contain the alcohol functional group.The chain carbons are numbered so as to provide least numeral position towards the end in vicinity to
In alkanes, the positions of side chains or alkyl substituents are indicated by lowest numeral places before prefix.

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Chapter 8 Solutions
ORGANIC CHEMISTRY (LL)-PACKAGE
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- In the drawing area below, draw the major products of this organic reaction: If there are no major products, because nothing much will happen to the reactant under these reaction conditions, check the box under the drawing area instead. 1. NaH 2. CH3Br ? Click and drag to start drawing a structure. No reaction. : ☐ Narrow_forward+ Predict the major product of the following reaction. : ☐ + ☑ ค OH H₂SO4 Click and drag to start drawing a structure.arrow_forwardConsider this organic reaction: ... OH CI Draw the major products of the reaction in the drawing area below. If there won't be any major products, because this reaction won't happen at a significant rate, check the box under the drawing area instead. ☐ No Reaction. Click and drag to start drawing a structure. : аarrow_forward
- Consider the following reactants: Br Would elimination take place at a significant rate between these reactants? Note for advanced students: by significant, we mean that the rate of elimination would be greater than the rate of competing substitution reactions. yes O no If you said elimination would take place, draw the major products in the upper drawing area. If you said elimination would take place, also draw the complete mechanism for one of the major products in the lower drawing area. If there is more than one major product, you may draw the mechanism that leads to any of them. Major Products:arrow_forwardDraw one product of an elimination reaction between the molecules below. Note: There may be several correct answers. You only need to draw one of them. You do not need to draw any of the side products of the reaction. OH + ! : ☐ + Х Click and drag to start drawing a structure.arrow_forwardFind one pertinent analytical procedure for each of following questions relating to food safety analysis. Question 1: The presence of lead, mercury and cadmium in canned tuna Question 2: Correct use of food labellingarrow_forward
- Formulate TWO key questions that are are specifically in relation to food safety. In addition to this, convert these questions into a requirement for chemical analysis.arrow_forwardWhat are the retrosynthesis and forward synthesis of these reactions?arrow_forwardWhich of the given reactions would form meso product? H₂O, H2SO4 III m CH3 CH₂ONa CH3OH || H₂O, H2SO4 CH3 1. LiAlH4, THF 2. H₂O CH3 IVarrow_forward
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