(a)
Interpretation:
The name of the given compound has to be given.
Concept Introduction:
The hydrocarbons which contain only single bonds are said to be
The Alkanes are named following some rules:
- The name of the alkane is given by the number of carbon atoms present in the chain. It is said to be Root of the alkane.
Root = number of carbon atoms in chain.
- To name the root, for one carbon atom, the root name use is meth-. For two carbon atoms, the root name is eth-, for three carbon atoms, it is prop-, for four carbon atoms, it is but-, for five carbon atoms, it is pent- and so on.
- The root name is followed by Suffix. Suffix indicates the
functional group present in the compound. It is placed after the root name.
Suffix = name of the functional group present in the compound.
- The root name also contains Prefix. Prefix is the groups attached to the root. It indicates the branched carbon atoms on the root chain and name according to the root specifying the carbon number on which it is placed. It contains –yl in name end. The prefix is placed before the root name.
Prefix = name of the branched carbon atoms on chain.
- The name of the alkane is given in the form
Prefix + Root + Suffix
(b)
Interpretation:
The name of the given compound has to be given.
Concept Introduction:
The hydrocarbons which contain only single bonds are said to be cycloalkanes. The general formula for alkanes can be given as
The cycloalkanes are named following some rules:
- The name of the alkane is given by the number of carbon atoms present in the ring. It is said to be Root of the alkane.
Root = number of carbon atoms in ring.
- To name the root, for one carbon atom, the root name use is meth-. For two carbon atoms, the root name is eth-, for three carbon atoms, it is prop-, for four carbon atoms, it is but-, for five carbon atoms, it is pent- and so on.
- The root name is followed by Suffix. Suffix indicates the functional group present in the compound. It is placed after the root name.
Suffix = name of the functional group present in the compound.
- The root name also contains Prefix. Prefix is the groups attached to the root. It indicates the branched carbon atoms on the root chain and name according to the root specifying the carbon number on which it is placed. It contains –yl in name end. The prefix is placed before the root name.
Prefix = name of the branched carbon atoms on chain.
- The name of the alkane is given in the form
Prefix + Root + Suffix
(c)
Interpretation:
The structure of the given compound (1,2-diethylcyclopentane) has to be drawn.
Concept Introduction:
The structure of the compound is given by its systematic name.
To give the structure from the name of the compound, the root name has to be identified. The root name indicates the number of carbon atoms present in the longest chain.
Then the functional group (suffix) has to be identified. It indicates whether any functional groups are present in the compound, it also gives whether the compound is an alkane or
The prefix of the name indicates the branched groups and their positions on the carbon chain.
The name of the compound is in the form
Prefix + Root + Suffix
(b)
Interpretation:
The structure of the given compound (2,4,5-trimethylnonane) has to be drawn.
Concept Introduction:
The structure of the compound is given by its systematic name.
To give the structure from the name of the compound, the root name has to be identified. The root name indicates the number of carbon atoms present in the longest chain.
Then the functional group (suffix) has to be identified. It indicates whether any functional groups are present in the compound, it also gives whether the compound is an alkane or alkene or alkyne.
The prefix of the name indicates the branched groups and their positions on the carbon chain.
The name of the compound is in the form
Prefix + Root + Suffix
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Chapter 15 Solutions
CHEMISTRY: MOLECULAR...(LLF) W/CONNECT
- Use the literature Ka value of the acetic acid, and the data below to answer these questions. Note: You will not use the experimental titration graphs to answer the questions that follow. Group #1: Buffer pH = 4.35 Group #2: Buffer pH = 4.70 Group #3: Buffer pH = 5.00 Group #4: Buffer pH = 5.30 Use the Henderson-Hasselbalch equation, the buffer pH provided and the literature pKa value of acetic acid to perform the following: a) calculate the ratios of [acetate]/[acetic acid] for each of the 4 groups buffer solutions above. b) using the calculated ratios, which group solution will provide the best optimal buffer (Hint: what [acetate]/[acetic acid] ratio value is expected for an optimal buffer?) c) explain your choicearrow_forwardHow would you prepare 1 liter of a 50 mM Phosphate buffer at pH 7.5 beginning with K3PO4 and 1 M HCl or 1 M NaOH? Please help and show calculations. Thank youarrow_forwardDraw the four most importantcontributing structures of the cation intermediate thatforms in the electrophilic chlorination of phenol,(C6H5OH) to form p-chlorophenol. Put a circle aroundthe best one. Can you please each step and also how you would approach a similar problem. Thank you!arrow_forward
- A 100mM lactic acid/lactate buffer was found to have a lactate to lactic acid ratio of 2 and a pH of 4.2. What is the pKa of lactic acid? Can you please help show the calculations?arrow_forwardUsing line angle formulas, draw thestructures of and name four alkanes that have total of 7carbons, one of which is tertiary.Please explain this in detail and can you also explain how to approach a similar problem like this as well?arrow_forwardUsing dashed line wedge projections drawthe indicated compounds and indicate whether thecompound you have drawn is R or S.(a) The two enantiomers of 2-chlorobutane. Can you please explain your steps and how you would approach a similar problem. Thank you!arrow_forward
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