The answer is given in the attachment.
Warm up 1. Identify if each compound below is a primary, secondary, or tertiary alkyl halide....
Categorise this alkyl halide as primary / secondary / tertiary, and identify the most electrophilic (8+) location within the molecule. a Br е Select one: Secondary alkyl halide; the electrophilic location is b Secondary alkyl halide; the electrophilic location is a Tertiary alkyl halide; the electrophilic location is a Primary alkyl halide; the electrophilic location is a 0 Tertiary alkyl halide; the electrophilic location is e
Draw the structural formula for a compound that contains a tertiary alcohol, a secondary alkyl halide, and primary, secondary and tertiary hydrogens. a. Indicate the number of beta-hydrogens relative the alkyl halide. b. Name the compound you just drew.
Substitution Problems I. In each of the problems below, label the alkyl halide as primary, secondary, or tertiary. Label the nucleophile as strong or weak. Decide whether an SN2 or an Sy1 reaction occurs. After, show the mechanism and product or products. Indicate stereochemistry where appropriate. a. Reaction of 1-bromopropane and sodium methoxide in methanol CH3 Na CH,Oн Br b. Reaction of 2-bromopropane in ethanol CH3CH2OH Br c. Reaction of (R) 3-chloro-3-methyl heptane in acetic acid Ci Cн CH,COOH но...
16.) Within each of the following sets of alkyl radicals, name each radical; identify each as either primary, secondary, or tertiary; rank in order of decreasing stability; and sketch an orbital picture of the most stable radical, showing the hyper conjugative interaction(s). (a) CH3CH2C·HCH3 and CH3CH2CH2CH2 · (b) (CH3CH2)2CHCH2 · and (CH3CH2)2C·CH3 (c) (CH3)2CHC·HCH3 , (CH3)2C·CH2CH3 and (CH3)2CHCH2CH2· (I put the lone electron after the radical carbon.) Also, my main question is in bold. The rest I know and understand....
HO Regarding the following reaction: 1) a. Classify the alkyl halide as tertiary, secondary, or primary. b. Based on your answers to la, deduce whether the alkyl halide would be suitable for (i) only S2 reactions, (ii) only Ss 1 reactions, or (1) both/either S2 or S1 reactions. 2) a. Classify the nucleophile (the electron-sharer) as either strong or weak b. Based on your answer to 2a, deduce whether the nucleophile would be suitable for (i) only Sw2 reactions, (1)...
16. Within each of the following sets of alkyl radicals, name each radical; identify each as either primary, secondary, or tertiary; rank in order of decreasing stability; and sketch an orbital picture of the most stable radical, showing the hyperconjugative interaction(s). a. CH,CHCHCH, and CH CH.CH,CH, b. (CH,CH),CHCH2- and (CH,CH2),ċCH, (CH),CHCHCH3, (CH),"CH,CH, and (CH3),CHCHCH:
pleas help 5,6,7,8,9,10 III IV 5. The product of free-radical halogenation reactions is an alkyl halide. The major amount of this halide forms during the second step of propagation. However, you should be aware that one possible termination step also forms alkyl halides. Why does the majority of the alkyl halide product come from the propagation step and not the termination step? A. At any given time during the reaction, the concentration of both the alkyl radical and the halide...
Substitution Problems I. In each of the problems below, label the alkyl halide as primary, secondary, or tertiary, Label the nucleophile as strong or weak. Decide whether an S2 or an Sol reaction occurs. Alter, show the mechanism and product or products. Indicate stereochemistry where appropriate. a. Reaction of 1-bromopropane and sodium methoxide in methanol + Na CH₂ CH OH b. Reaction of 2-bromopropane in ethanol Br + CH.CH, OH - c. Reaction of (R) 3-chloro-3-methylheptane in acetic acid CH3...
Item 5 Label each hydrogen atom in the given compound as primary, secondary, or tertiary. Identify the appropriate atoms by selecting each atom and assigning it a map number of 1 for primary hydrogen atoms, ar tertiary hydrogen atoms. To do this, right click on an atom and choose Atom Properties. (Mac users: Use an equivalent for entering a value. DOB , H:120 6 + \33
ChemActivity 10: Oxidation and Reduction 145 Model 7: Primary (1°), Secondary (2°), and Tertiary (3°) Carbons The words methyl (0'), primary (1), secondary (2"), and tertiary (3) were used to describe the number of (nonhydrogen) R groups attached to a carbocation carbon (see CA 8). This same naming strategy is used to describe any carbon with one attached "heteroatom," Z (hetero other). H R Z any atom other than C or H (hetroatom) R- -z -Z н- alkyl (not H)...