
Concept explainers
Interpretation:
The structural formulas for given compounds are to be written.
Concept introduction:
The longest chain is termed as the parent chain, which is then numbered from the end that the substituted carbons get a lower number. The name and number of substituents are then prefixed to the name of the parent chain.
In chemical nomenclature, the
The parent chain is the longest continuous chain of carbon atoms.
The parent chain is numbered from that end which is closest to the substituent.
If the same substituent occurs more than once, the location of each point on which the substituent occurs is given.
If there are two or more different substituents they are listed in alphabetical order using the base name
The name of the
A structural formula is the formula thatprovides an insight into the structure of the compound. It shows all the substituents and
The structure can be easily written from the systematic name. The parent chain is at first drawn and numbered from any end.
Thereafter, the name is written thatincludes the name and the number of substituents. The substituents are written with their number in alphabetical order followed by the name of the parent chain and the functional group as a suffix.
The suffix –olis used for the alcohol group.
The suffix –al is used for the aldehyde group.
The suffix –one is used for the ketone group.
The –e ending of an alkane is replaced by –amine for amine functional group.
The suffix amide is then added for the amide group.
The suffix -oate is used for the ester.
Functional groups are specific substituent within the molecules that are responsible for the characteristic
Esters are the organic compounds thatcontain
Alcohols are the organic compounds thatcontain
Amides are the organic compounds thatcontain

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Chapter 25 Solutions
Chemistry
- ↓ ina xSign x Sign X labs X Intro X Cop Xa chat X My Cx Grac X Laur x Laur xash learning.com/ihub/assessment/f188d950-dd73-11e0-9572-0800200c9a66/d591b3f2-d5f7-4983-843c-0d00c1c0340b/f2b47861-07c4-4d1b-a1ee-e7db2 +949 pts /3400 K Question 16 of 34 > © Macmillan Learning Draw the major E2 reaction product formed when cis-1-chloro-2-ethylcyclohexane (shown) reacts with hydroxide ion in DMSO. H CH2CH3 H H HO- H H H Cl DMSO H H C Select Draw Templates More C H 0 2 Erasearrow_forwardA common buffer for stabilizing antibodies is 100 mM Histidine at pH 7.0. Describe the preparation of this buffer beginning with L-Histidine monohydrochloride monohydrate and 1 M NaOH. Be certain to show the buffering reaction that includes the conjugate acid and base.arrow_forwardFina x | Sign X Sign X lab: X Intro X Cop) X a chat x My x Grad xLaur x Laur x a sheg X S Shoj XS SHE X acmillanlearning.com/ihub/assessment/f188d950-dd73-11e0-9572-0800200c9a66/d591b3f2-d5f7-4983-843c-0d00c1c0340b/f2b47861-07c4-4d1b-a1ee-e7db27d6b4ee?actualCourseld=d591b3f2- 5 © Macmillan Learning Organic Chemistry Maxwell presented by Macmillan Learning For the dehydrohalogenation (E2) reaction shown, draw the Zaitsev product, showing the stereochemistry clearly. H H KOH Br EtOH Heat Select Draw Templates More Erase // C H Q Search hp Q2 Q Δ קו Resouarrow_forward
- Is the structural form shown possible given the pKa constraints of the side chains?arrow_forwardon x Fina X Sign X Sign x lab X Intro X Cop X chat X My x Grac x Laur x Laur x ashes x S Shox S SHE x a eve.macmillanlearning.com/ihub/assessment/f188d950-dd73-11e0-9572-0800200c9a66/d591b3f2-d5f7-4983-843c-0d00c1c0340b/f2b47861-07c4-4d1b-a1ee-e7db27d6b4ee?actualCourseld=d591b3f2-c stions estion. ct each urces. +95 Macmillan Learning Draw the product formed by the reaction of potassium t-butoxide with (15,25)-1-bromo-2-methyl-1-phenylbutane (shown). Clearly show the stereochemistry of the product. H BH (CH3)3CO-K+ +100 H3CW (CH3)3COH +85 H3CH2C +95 ossible ↓ Q Search Select Draw Templates More C H 0 bp A Erase 2Q 112 Resouarrow_forwardIdentify the structure of the PTH derivative generated after two rounds of Edman degradation.arrow_forward
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