Concept explainers
Interpretation:
The name of the given
Concept Introduction:
In order to give the IUPAC name to the branched-chain alkane following steps are followed:
1. The parent (longest) continuous carbon chain is identified.
2. The ending of the parent chain for alkane (-e) is -ane.
3. Name should be written in alphabetical order and numbering should be done in such a way that the substituent group gets lowest number.
4. Hyphen is used to connect the number to the name.
For number of carbons atoms in alkane chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec.
Interpretation:
The name of the given alkane should be determined.
Concept Introduction:
In order to give the IUPAC name to the branched-chain alkane following steps are followed:
1. The parent (longest) continuous carbon chain is identified.
2. The ending of the parent chain for alkane (-e) is -ane.
3. Name should be written in alphabetical order and numbering should be done in such a way that the substituent group gets lowest number.
4. Hyphen is used to connect the number to the name.
For number of carbons atoms in alkane chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec.
Interpretation:
The name of the given alkane should be determined.
Concept Introduction:
In order to give the IUPAC name to the branched-chain alkane following steps are followed:
1. The parent (longest) continuous carbon chain is identified.
2. The ending of the parent chain for alkane (-e) is -ane.
3. Name should be written in alphabetical order and numbering should be done in such a way that the substituent group gets lowest number.
4. Hyphen is used to connect the number to the name.
For number of carbons atoms in alkane chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec.
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Chapter 20 Solutions
EBK INTRODUCTORY CHEMISTRY
- Examine the reaction below. Highlight all bonds that have broken in the reactant. Br H H₂C-C- -H 5 H-C-H H-C-H BIE 们 OH H H H₂C-C= H-C-H H-C-Harrow_forwardClassify each of the following as either a substitution, elimination, or addition reaction. CH3 CH3 CH2=CH₂ CH2=C-CH2-OH + Br₂ Br-CH2-C -CH₂-OH Br CH,CH3 CH3-C-CH-CH2-CH3 он ° CH₂ HO C-C-CH3 + NH3 CH₂ он CH3-CH-O-CH3 O-CH3 CH3-C-CH3 + H₂O O-CH3 CH3CH₂ H + H₂O CH3-C=C-CH2-CH3 • CHI Δ Å CH CH3 H+ CH3 C-H + HO-CH3 H" Q-CH₂ CH3-C-CH3 + HO-CH3 OH O substitution O elimination addition substitution O elimination addition O substitution elimination addition O substitution O elimination addition substitution O elimination 00 additionarrow_forwardSearch 5:45 PM Sun Dec 15 Quiz 9 ... ล 25%0 A Done Quiz #9 = Name: Draw the major products of the following. Show Stereochemistry when applicable: 1. OsO4 A 2. NaHSO 3, H 20 Cl₂ ➤ C H2, Pd/C E HBr 1. Hg(OAc) 2, H₂O 2. NaBH 4 Ꭰ KI, H3PO4 F KMnO4, H3O+ KMnO4, H2O G H HBr Br2 J CH2N2 ➤ K CH2I2, Zn(Cu) Cl2, CH3OH C 1. 03 2. Zn, H3O+ HCI 1. BH 3 N M 2. NaOH, H 202 KMnO4, NaOH H₂O P Br2, H2O R 1. BH 3 2. NaOH, H 202 Cl2, CH3CH2OH Tarrow_forward
- Select the stronger base: H-CEN equally basic H H H H-C-N H Select the stronger acid: Select the stronger base: Select the stronger base: H -H equally acidic о equally basic NH equally basic оarrow_forwardClassify each of the following as either a substitution, elimination, or addition reaction. CH3 CH3 CH3-CH-CH2-C-CH3 + Br₂ CH3 CH3 CH3 CH3-C-CH2-C-CH3 + HBr substitution ○ elimination Br CH3 CHI CHO CHA HO CH он Cl CH3-CH2-CH-CH2-CH3 CH₂ DBU H* - CHI CHO CH3 + H2O Ӧ CH3 CH3-CH2-CH=CH-CH3 + HCI OH Pd/C CH3 CH3-CH-CH2-C-CH3 CH3 H C-CH2-CH3 + HO-CH3 addition substitution elimination ○ addition ○ substitution ○ elimination O addition substitution O elimination addition substitution O elimination addition CH3 C-CH3 + H2 CH3 CH3-O-CH-CH2-CH3 Онarrow_forward=> (8 pts) Use retrosynthetic analysis (that is, use retrosynthetic arrows as was done in class) to suggest a synthesis route for the transformation shown below. Sear bonsarrow_forward
- d) 1. Complete the following reactions; all reactions are at room temperature. No heat is involved here. Show Major product only. Indicate the type of mechanism: SN1 or SN2. (1 pt each) a) Br + b) Br e) OH CH3DH + H20 он HCJ Zn Cl₂ OH + HCI 20 C12 + H-Brarrow_forwardWhat is the IUPAC name for the compound shown? LOH IUPAC name: BIU X2 x²arrow_forwardDon't used Ai solutionarrow_forward
- 2. Write the IUPAC name of the major product that would be obtained from the dehydration of 3,5-dimethylcyclohexanol. What is the type mechanism of the reaction (E1, E2, SN1, SN2)? Draw the detailed mechanism of the reaction. (2.5 pts) 3. In Experiment 8, You synthesized n-butyl bromide using sodium bromide, sulfuric acid and butyl alcohol. (2.5 pts) a. Write the detailed mechanism of this reaction indicating what type of mechanism is this reaction. b. What will happen to the rate of the reaction if NaCl was used instead of NaBr? c. What will be the mechanism of the reaction if t-butyl alcohol is used with NaBr in presence of sulfuric acid? Draw detailed mechanism.arrow_forwardIn each row of the table below, select the stronger acid or base, as instructed. The most acidic H atom in each acid has been highlighted. Select the stronger acid: Select the stronger acid: Select the stronger base: Select the stronger base: H H Tx NH equally acidic equally acidic H equally basic equally basicarrow_forwardPlease correct answer and don't used hand raitingarrow_forward
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