endstream Combustion Alkane + O 2 → CO 2 + H 2 O 2. (at least one alkene is formed). Groups that are trans on the alkene will end up trans on the cyclopropane product. It would have to have two groups attached to show cis-trans isomerism. 5 0 obj 4�.0,` �3p� ��H�.Hi@�A>� Draw the line bond structures for the following alkenes, cyclic alkenes, and alkynes: a) noncyclic alkenes that contain 4 carbon atoms (3 possible) b) cyclic alkenes that contain 4 carbon atoms (4 possible) c) alkynes that contain 4 carbon atoms (2 possible, neither of them is a cyclic alkyne) 2. endobj �FV>2 u�����/�_$\�B�Cv�< 5]�s.,4�&�y�Ux~xw-bEDCĻH����G��KwF�G�E�GME{E�EK�X,Y��F�Z� �={$vr����K���� ��K0ށi���A����B�ZyCAP8�C���@��&�*���CP=�#t�]���� 4�}���a � ��ٰ;G���Dx����J�>���� ,�_“@��FX�DB�X$!k�"��E�����H�q���a���Y��bVa�bJ0՘c�VL�6f3����bձ�X'�?v 6��-�V`�`[����a�;���p~�\2n5��׌���� �&�x�*���s�b|!� %PDF-1.3 Worksheet will open in a new window. Some of the worksheets for this concept are Alkanes and alkenes work, Alkenes and alkynes work, Work naming and drawing alkanes, Work alkenes, Naming and drawing alkenes work and key, Chapter 8, Naming organic compounds alkanes, Chapter 1 organic compounds alkanes. Groups that are cis on the alkene will end up cis on the cyclopropane product. The halogens are F 2, Cl 2, Br 2, I 2. Found worksheet you are looking for? 2. 1) o hcl ch3oh 2) hcl ch3 3) hcl 4) hcl 5) hbr 6) hcl 7) ch3 h3o + 8) h3o + 9) h3o + 10) hg(oac)2, h2o nabh4 ch3 11) hg(oac)2, h2o nabh4. Cracking Cracking breakes a big molecule into smaller molecules. Example: Terminal alkynes form insoluble metal acetylides and precipate 13) Attack on the less sterically hindered primary bromide (bromoethane) is more favorable. stream >> We will review their nomenclature, and also learn about the vast possibility of reactions using alkenes and alkynes as starting materials. This interactive quiz and worksheet combo will test how much you know about the type of organic chemical compounds called alkynes. Example: Methane + chlorine → chloromethane + hydrogen chloride 3. 1637 3/k��E�h�� ��s�H)+Ǣ��r0±[�hi �Y#�G�0���3FvafGH�/Ӫ�� ��.UŚ9��F��K!�%�˛�B�m�#CjS%|F�FV �1��>0Ǯ��׶�ӵ���̎�4���aׂ�C�d�b��Rñ���+��ē���3��+���� ���ӓ b~� U# &�Z���t]�,:F�����!n�+ٿ%���J�E�k"WG���cH_w�j�A������%�CX�_9˽����r䐵VRV��eį�}"7� To download/print, click on pop-out icon or print icon to worksheet to print or download. 12) hg(oac)2, ch3oh nabh 4 13) ch3 bh3 thf /TT2 9 0 R /TT8 15 0 R /TT12 19 0 R /TT10 17 0 R /TT6 13 0 R >> >> 4-methyl-1-pentyne 3. You can & download or print using the browser document reader options. E�6��S��2����)2�12� ��"�įl���+�ɘ�&�Y��4���Pޚ%ᣌ�\�%�g�|e�TI� ��(����L 0�_��&�l�2E�� ��9�r��9h� x�g��Ib�טi���f��S�b1+��M�xL����0��o�E%Ym�h�����Y��h����~S�=�z�U�&�ϞA��Y�l�/� �$Z����U �m@��O� � �ޜ��l^���'���ls�k.+�7���oʿ�9�����V;�?�#I3eE妧�KD����d�����9i���,�����UQ� ��h��6'~�khu_ }�9P�I�o= C#$n?z}�[1 {�KFE,��W5��eoY�WM���. endobj alkene reactions and mechanisms for questions 1-24, give the major organic product of the reaction, paying particular attention to regio- and stereochemical outcomes. Ⱦ�h���s�2z���\�n�LA"S���dr%�,�߄l��t� << /Length 24 0 R /Filter /FlateDecode >> 23 0 obj << /ProcSet [ /PDF /Text ] /ColorSpace << /Cs1 7 0 R >> /Font << /TT4 11 0 R Reactions of Alkanes 1. Key Takeaway • Alkynes are hydrocarbons with carbon-to-carbon triple bonds and properties %��������� O*��?�����f�����`ϳ�g���C/����O�ϩ�+F�F�G�Gό���z����ˌ��ㅿ)����ѫ�~w��gb���k��?Jި�9���m�d���wi獵�ޫ�?�����c�Ǒ��O�O���?w| ��x&mf������ 2612 stream endstream Reaction of an alkynide with the secondary (hindered) bromide would result mostly in elimination instead of substitution. Displaying top 8 worksheets found for - Alkanes And Alkenes. << /Type /Page /Parent 3 0 R /Resources 6 0 R /Contents 4 0 R /MediaBox [0 0 612 792] endobj Alkenes and Alkynes Worksheet and Key 1. x�Z;��6��+x����'-���ϸIg`�8�)�0��I�����"{�i�8��|�O��$�//�:��������3�j�^W��|�����Ҽu"���˸F6�ְ�P;��=x��+�E��'҂`�y��4l�4o��{�>�~z�j�.ة��7���������ǧQ�ɯ5�UMݝw? 6 0 obj About This Quiz & Worksheet. The cyclopropanation reaction of an alkene with a carbene takes place in a single step. Alkenes and alkynes can be transformed into almost any other functional group you can name! ��OE�S�K���A��ѻT6B�@�MM��\Τ7�{ǢO�M ���!�B�8Ẍ́��](^�NĂGGq�ˊK��c'�D���"Yz���k?��A����s�[m$Xt.����]Q�����R.��V��xZAA��Ф��``�lc���Q�ECW�Ea>XC����`��iʁ�uC�('�I�{��o� �k ��c!��y^ stream 21 0 obj Displaying top 8 worksheets found for - Alkanes And Alkenes. There is NO intermediate. Acid-base reaction 2) 11) B 12) Add a solution of Cu+ or Ag+. endobj 14) 7 0 obj 1. {�%P �*�ª(w����';"N�i�+�h�c��HI^�N]��߅H���D�&�?��L�t�`cn�� ��^���(n���&�Ht0Xl��F�NKň�21 ,���X:�-_�9�TC���Y��K�I�M��S�=. ��.3\����r���Ϯ�_�Yq*���©�L��_�w�ד������+��]�e�������D��]�cI�II�OA��u�_�䩔���)3�ѩ�i�����B%a��+]3='�/�4�0C��i��U�@ёL(sYf����L�H�$�%�Y�j��gGe��Q�����n�����~5f5wug�v����5�k��֮\۹Nw]������m mH���Fˍe�n���Q�Q��`h����B�BQ�-�[l�ll��f��jۗ"^��b���O%ܒ��Y}W�����������w�vw����X�bY^�Ю�]�����W�Va[q`i�d��2���J�jGէ������{�����׿�m���>���Pk�Am�a�����꺿g_D�H��G�G��u�;��7�7�6�Ʊ�q�o���C{��P3���8!9������-?��|������gKϑ���9�w~�Bƅ��:Wt>���ҝ����ˁ��^�r�۽��U��g�9];}�}��������_�~i��m��p���㭎�}��]�/���}������.�{�^�=�}����^?�z8�h�c��' x�ZK��6��W0���5MR|�ݤ����lO� � ��P�%Qk�Z���^Z�4�o�C�d_�Ov��K��_L��=’�J�/�3��=�`��̙�7�0�� ����v:����/���/�@l��!��︰K/����f�>��LJ^�> ��.G��u`�����s��ZݤR�K�[Œn �vw�+�����EI��4�Yodi����FFA#��;onU�ͽZ�����.�����&O�K3�m��ԤcM��(�!P�C)ϝ�i ����5������̀�B�O -n��D����9 v����?4���l�_��l##����F)E��Ґ�=����%1��H"4�8��,�Ep�r��P� D�;4K�ʃ�;�-Z�ߡ�0�Z~�E3 ����9� �?OdW�.W]�6Nj4>A _�,�i1�-~��ח`G&ب0��ʕ���h�D��q'g�ob���q%I�gw*�y�$���u1Fξ�t^'�P\�j&q��:�5D&ीG�M�v��-�A���B�_��IǨ��=�B(�ip�/-�L�\0~�絀K�[���%��mr��Q0�����`����I�^$o�� ]���ޞ%:�yz�H��!3�M4+�Pm0�b3��y���x"��G!�EBC��[�5EE�����I� ϩ� 5p���.��wkb�З䓦�*�봡y�x]a���)Io��}E(��5���ȨG(Zs+4k9$�Q�::7�k 1����������-�1�v�AEy}ؠ�r��9`T��}�/�*�Cd�EV�mV���F��Me��²A�Q����L��������t��un�uTb )��K���kG鑈$,{���"�"�؂����쬞d�M�g���Z�:�(��R��D����H׈�Ԓ?�F��t[虖z,��zy��kO|��X��Gh��lL��Dc�����}��;l�6�}�*��ώ�cWm2�šC��y�=Q��,o�U��Pَ1�o��^���hD��U�F�A���d@kp��� Tt"ԕ�YW��HG��6��f�TxE� i�x�$� �I�03'�hv�4�Xb�63�l8��ŵD.�P�3|ր֏^vHT����, [ /ICCBased 20 0 R ] endobj Both undergo addition reactions. endobj 20 0 obj 4 0 obj [7A�\�SwBOK/X/_�Q�>Q�����G�[��� �`�A�������a�a��c#����*�Z�;�8c�q��>�[&���I�I��MS���T`�ϴ�k�h&4�5�Ǣ��YY�F֠9�=�X���_,�,S-�,Y)YXm�����Ěk]c}džj�c�Φ�浭�-�v��};�]���N����"�&�1=�x����tv(��}�������'{'��I�ߝY�)� Σ��-r�q�r�.d.�_xp��Uە�Z���M׍�v�m���=����+K�G�ǔ����^���W�W����b�j�>:>�>�>�v��}/�a��v���������O8� � ߏƿ'� Zk�!� $l$T����4Q��Ot"�y�\b)���A�I&N�I�$R$)���TIj"]&=&�!��:dGrY@^O�$� _%�?P�(&OJEB�N9J�@y@yC�R �n�X����ZO�D}J}/G�3���ɭ���k��{%O�חw�_.�'_!J����Q�@�S���V�F��=�IE���b�b�b�b��5�Q%�����O�@��%�!BӥyҸ�M�:�e�0G7��ӓ����� e%e[�(����R�0`�3R��������4�����6�i^��)��*n*|�"�f����LUo�՝�m�O�0j&jaj�j��.��ϧ�w�ϝ_4����갺�z��j���=���U�4�5�n�ɚ��4ǴhZ�Z�Z�^0����Tf%��9�����-�>�ݫ=�c��Xg�N��]�. No; a triply bonded carbon atom can form only one other bond. 2 0 obj Alkenes have double bonds; alkynes have triple bonds. Some of the worksheets for this concept are Alkanes and alkenes work, Alkenes and alkynes work, Work naming and drawing alkanes, Work alkenes, Naming and drawing alkenes work and key, Chapter 8, Naming organic compounds alkanes, Chapter 1 organic compounds alkanes. << /Length 21 0 R /N 3 /Alternate /DeviceRGB /Filter /FlateDecode >> << /Length 5 0 R /Filter /FlateDecode >> Substitution Reaction Reaction by a halogen in presence of UV light. endobj A1�v�jp ԁz�N�6p\W� p�G@ x��wTS��Ͻ7��" %�z �;HQ�I�P��&vDF)VdT�G�"cE��b� �P��QDE�݌k �5�ޚ��Y�����g�}׺ P���tX�4�X���\���X��ffG�D���=���HƳ��.�d��,�P&s���"7C$ As such, the geometry of the alkene is preserved in the product.

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